Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[One patient was found to have Leigh syndrome due to a mutation in MT-ATP6, two affected siblings were discovered to be compound heterozygous for mutations in the NDUFV1 gene, which causes mitochondrial complex I deficiency, and one patient was found to have coenzyme Q10 deficiency due to compound heterozygous mutations in COQ2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP383733.RA9wiD6M8wNeYEGhs5tOqcqRq6ZsgkqqczbyScfyPm2h0130_assertion description "[One patient was found to have Leigh syndrome due to a mutation in MT-ATP6, two affected siblings were discovered to be compound heterozygous for mutations in the NDUFV1 gene, which causes mitochondrial complex I deficiency, and one patient was found to have coenzyme Q10 deficiency due to compound heterozygous mutations in COQ2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP383733.RA9wiD6M8wNeYEGhs5tOqcqRq6ZsgkqqczbyScfyPm2h0130_provenance.
• NP356693.RAvA4LZpDxQfBQFt2BOn2eR0Fr_7T9xlcB_cwMdWzv28c130_assertion description "[One patient was found to have Leigh syndrome due to a mutation in MT-ATP6, two affected siblings were discovered to be compound heterozygous for mutations in the NDUFV1 gene, which causes mitochondrial complex I deficiency, and one patient was found to have coenzyme Q10 deficiency due to compound heterozygous mutations in COQ2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP356693.RAvA4LZpDxQfBQFt2BOn2eR0Fr_7T9xlcB_cwMdWzv28c130_provenance.
• NP593841.RACwq-sEhWJSqzH6Xh_y8TDaeJFI_bVrkbsDnjll6dYGg130_assertion description "[One patient was found to have Leigh syndrome due to a mutation in MT-ATP6, two affected siblings were discovered to be compound heterozygous for mutations in the NDUFV1 gene, which causes mitochondrial complex I deficiency, and one patient was found to have coenzyme Q10 deficiency due to compound heterozygous mutations in COQ2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP593841.RACwq-sEhWJSqzH6Xh_y8TDaeJFI_bVrkbsDnjll6dYGg130_provenance.
• NP657446.RAtQIDMlSd8U9KW9sklhTlvnmG_nD10JDtDkrx8i0QD-8130_assertion description "[One patient was found to have Leigh syndrome due to a mutation in MT-ATP6, two affected siblings were discovered to be compound heterozygous for mutations in the NDUFV1 gene, which causes mitochondrial complex I deficiency, and one patient was found to have coenzyme Q10 deficiency due to compound heterozygous mutations in COQ2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP657446.RAtQIDMlSd8U9KW9sklhTlvnmG_nD10JDtDkrx8i0QD-8130_provenance.
• NP657858.RAnlth6yVtO_Yfqwg4AnkIDE83mD_ThAVuyAovBgvMYpg130_assertion description "[One patient was found to have Leigh syndrome due to a mutation in MT-ATP6, two affected siblings were discovered to be compound heterozygous for mutations in the NDUFV1 gene, which causes mitochondrial complex I deficiency, and one patient was found to have coenzyme Q10 deficiency due to compound heterozygous mutations in COQ2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP657858.RAnlth6yVtO_Yfqwg4AnkIDE83mD_ThAVuyAovBgvMYpg130_provenance.
• NP872893.RAV0EnxJq3N8cHXu6XUnEb80eKuo-zU3JSrz6g8JLm4kg130_assertion description "[One patient was found to have Leigh syndrome due to a mutation in MT-ATP6, two affected siblings were discovered to be compound heterozygous for mutations in the NDUFV1 gene, which causes mitochondrial complex I deficiency, and one patient was found to have coenzyme Q10 deficiency due to compound heterozygous mutations in COQ2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP872893.RAV0EnxJq3N8cHXu6XUnEb80eKuo-zU3JSrz6g8JLm4kg130_provenance.
• NP312781.RA1HdpC-OWakflt4eSk8ZgJ48YahU4nweHhw0VbFYWG6g130_assertion description "[One patient was found to have Leigh syndrome due to a mutation in MT-ATP6, two affected siblings were discovered to be compound heterozygous for mutations in the NDUFV1 gene, which causes mitochondrial complex I deficiency, and one patient was found to have coenzyme Q10 deficiency due to compound heterozygous mutations in COQ2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP312781.RA1HdpC-OWakflt4eSk8ZgJ48YahU4nweHhw0VbFYWG6g130_provenance.
• NP711091.RAybrk1GA76wbbmENJjVGC0dg07opxozsR7miWRm9L8ds130_assertion description "[One patient was found to have Leigh syndrome due to a mutation in MT-ATP6, two affected siblings were discovered to be compound heterozygous for mutations in the NDUFV1 gene, which causes mitochondrial complex I deficiency, and one patient was found to have coenzyme Q10 deficiency due to compound heterozygous mutations in COQ2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP711091.RAybrk1GA76wbbmENJjVGC0dg07opxozsR7miWRm9L8ds130_provenance.
• NP586690.RAXTKli0KWwdiapsAAesxX3vDi1F_eE-L8A5hLR40RLj8130_assertion description "[One patient was found to have Leigh syndrome due to a mutation in MT-ATP6, two affected siblings were discovered to be compound heterozygous for mutations in the NDUFV1 gene, which causes mitochondrial complex I deficiency, and one patient was found to have coenzyme Q10 deficiency due to compound heterozygous mutations in COQ2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP586690.RAXTKli0KWwdiapsAAesxX3vDi1F_eE-L8A5hLR40RLj8130_provenance.
• NP480223.RAEFG_Q-ABpF6x_jUdMM7MyunpY9S5FF_1TmvTnZN-a8c130_assertion description "[One patient was found to have Leigh syndrome due to a mutation in MT-ATP6, two affected siblings were discovered to be compound heterozygous for mutations in the NDUFV1 gene, which causes mitochondrial complex I deficiency, and one patient was found to have coenzyme Q10 deficiency due to compound heterozygous mutations in COQ2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP480223.RAEFG_Q-ABpF6x_jUdMM7MyunpY9S5FF_1TmvTnZN-a8c130_provenance.
• assertion description "[One patient was found to have Leigh syndrome due to a mutation in MT-ATP6, two affected siblings were discovered to be compound heterozygous for mutations in the NDUFV1 gene, which causes mitochondrial complex I deficiency, and one patient was found to have coenzyme Q10 deficiency due to compound heterozygous mutations in COQ2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP887226.RAnzJDk_2PlnKMSpuW0pvfKAwQP5D78eQbJl5Ags6WYX4130_assertion description "[One patient was found to have Leigh syndrome due to a mutation in MT-ATP6, two affected siblings were discovered to be compound heterozygous for mutations in the NDUFV1 gene, which causes mitochondrial complex I deficiency, and one patient was found to have coenzyme Q10 deficiency due to compound heterozygous mutations in COQ2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887226.RAnzJDk_2PlnKMSpuW0pvfKAwQP5D78eQbJl5Ags6WYX4130_provenance.
• NP1073661.RApTMQMGWFkb_6KV5FRBqjEDdr5Vi7CHd_1wCLrs_gS7M130_assertion description "[One patient was found to have Leigh syndrome due to a mutation in MT-ATP6, two affected siblings were discovered to be compound heterozygous for mutations in the NDUFV1 gene, which causes mitochondrial complex I deficiency, and one patient was found to have coenzyme Q10 deficiency due to compound heterozygous mutations in COQ2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1073661.RApTMQMGWFkb_6KV5FRBqjEDdr5Vi7CHd_1wCLrs_gS7M130_provenance.
• NP1073664.RAo6bMpy7qaMqufB_0_Gmu-ZMUvwAeyPThtVoZZE10kqM130_assertion description "[One patient was found to have Leigh syndrome due to a mutation in MT-ATP6, two affected siblings were discovered to be compound heterozygous for mutations in the NDUFV1 gene, which causes mitochondrial complex I deficiency, and one patient was found to have coenzyme Q10 deficiency due to compound heterozygous mutations in COQ2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1073664.RAo6bMpy7qaMqufB_0_Gmu-ZMUvwAeyPThtVoZZE10kqM130_provenance.
• NP572562.RAw3jZtnYPPdJbC6MWnAIyKAnIDz-84w0cZ0uyV-nQUQA130_assertion description "[One patient was found to have Leigh syndrome due to a mutation in MT-ATP6, two affected siblings were discovered to be compound heterozygous for mutations in the NDUFV1 gene, which causes mitochondrial complex I deficiency, and one patient was found to have coenzyme Q10 deficiency due to compound heterozygous mutations in COQ2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP572562.RAw3jZtnYPPdJbC6MWnAIyKAnIDz-84w0cZ0uyV-nQUQA130_provenance.
• NP572624.RAyDABeD_GGdpb_C1qY2vPoxHxxwakdbYEcMrtBHSngjE130_assertion description "[One patient was found to have Leigh syndrome due to a mutation in MT-ATP6, two affected siblings were discovered to be compound heterozygous for mutations in the NDUFV1 gene, which causes mitochondrial complex I deficiency, and one patient was found to have coenzyme Q10 deficiency due to compound heterozygous mutations in COQ2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP572624.RAyDABeD_GGdpb_C1qY2vPoxHxxwakdbYEcMrtBHSngjE130_provenance.
• NP1073662.RAGa7_LeNqFp9e72qwNP7EzKeGFEnPlAHdA5CC7JALUO4130_assertion description "[One patient was found to have Leigh syndrome due to a mutation in MT-ATP6, two affected siblings were discovered to be compound heterozygous for mutations in the NDUFV1 gene, which causes mitochondrial complex I deficiency, and one patient was found to have coenzyme Q10 deficiency due to compound heterozygous mutations in COQ2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1073662.RAGa7_LeNqFp9e72qwNP7EzKeGFEnPlAHdA5CC7JALUO4130_provenance.
• NP1073663.RAHItCG08JGJRuAD_En8O1Tr433Tvz6Om3VIGgTGung3I130_assertion description "[One patient was found to have Leigh syndrome due to a mutation in MT-ATP6, two affected siblings were discovered to be compound heterozygous for mutations in the NDUFV1 gene, which causes mitochondrial complex I deficiency, and one patient was found to have coenzyme Q10 deficiency due to compound heterozygous mutations in COQ2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1073663.RAHItCG08JGJRuAD_En8O1Tr433Tvz6Om3VIGgTGung3I130_provenance.
• NP1073665.RA9K-wiiYuH9LEKO67mt21DKCYdKngkT_nDs9oaRR6nw4130_assertion description "[One patient was found to have Leigh syndrome due to a mutation in MT-ATP6, two affected siblings were discovered to be compound heterozygous for mutations in the NDUFV1 gene, which causes mitochondrial complex I deficiency, and one patient was found to have coenzyme Q10 deficiency due to compound heterozygous mutations in COQ2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1073665.RA9K-wiiYuH9LEKO67mt21DKCYdKngkT_nDs9oaRR6nw4130_provenance.
• NP887250.RA0IHRG4BrlY5FQiyviXqOmgpMibeC_kH9wIgU2jrvckY130_assertion description "[One patient was found to have Leigh syndrome due to a mutation in MT-ATP6, two affected siblings were discovered to be compound heterozygous for mutations in the NDUFV1 gene, which causes mitochondrial complex I deficiency, and one patient was found to have coenzyme Q10 deficiency due to compound heterozygous mutations in COQ2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887250.RA0IHRG4BrlY5FQiyviXqOmgpMibeC_kH9wIgU2jrvckY130_provenance.