Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Finally OPA1 missense mutations are involved in phenotypes presenting optic atrophy as a major feature.To define the relative contribution of POLG1, POLG2, ANT1 and PEO1 genes to the mtDNA multiple deletion syndromes, we analysed them in a cohort of 67 probands showing accumulation of multiple mtDNA deletions in muscle.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP622266.RACvFsUSZ1E3ZcLG9KE77NObY-bhMWiBCyu29Ao9zYumk130_assertion description "[Finally OPA1 missense mutations are involved in phenotypes presenting optic atrophy as a major feature.To define the relative contribution of POLG1, POLG2, ANT1 and PEO1 genes to the mtDNA multiple deletion syndromes, we analysed them in a cohort of 67 probands showing accumulation of multiple mtDNA deletions in muscle.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP622266.RACvFsUSZ1E3ZcLG9KE77NObY-bhMWiBCyu29Ao9zYumk130_provenance.
• NP547930.RAR5IMCHpPYG3S5oeiPRYQqMAJorOjN5zakSja81n4xD4130_assertion description "[Finally OPA1 missense mutations are involved in phenotypes presenting optic atrophy as a major feature.To define the relative contribution of POLG1, POLG2, ANT1 and PEO1 genes to the mtDNA multiple deletion syndromes, we analysed them in a cohort of 67 probands showing accumulation of multiple mtDNA deletions in muscle.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547930.RAR5IMCHpPYG3S5oeiPRYQqMAJorOjN5zakSja81n4xD4130_provenance.
• NP245608.RAqWpfPDdI1mgHGjXTJZuoYQHwzBm833uOFGR-9Hwlv5Y130_assertion description "[Finally OPA1 missense mutations are involved in phenotypes presenting optic atrophy as a major feature.To define the relative contribution of POLG1, POLG2, ANT1 and PEO1 genes to the mtDNA multiple deletion syndromes, we analysed them in a cohort of 67 probands showing accumulation of multiple mtDNA deletions in muscle.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP245608.RAqWpfPDdI1mgHGjXTJZuoYQHwzBm833uOFGR-9Hwlv5Y130_provenance.
• NP383438.RAbnFPDmQSfOwhsAsX1eWmqfqtX25gGz0Cake14n52g-Y130_assertion description "[Finally OPA1 missense mutations are involved in phenotypes presenting optic atrophy as a major feature.To define the relative contribution of POLG1, POLG2, ANT1 and PEO1 genes to the mtDNA multiple deletion syndromes, we analysed them in a cohort of 67 probands showing accumulation of multiple mtDNA deletions in muscle.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP383438.RAbnFPDmQSfOwhsAsX1eWmqfqtX25gGz0Cake14n52g-Y130_provenance.
• NP751331.RAs6hNj33ToYqCn-Zk-CQXZCS_uh3cKMi1P2OokNcZk-o130_assertion description "[Finally OPA1 missense mutations are involved in phenotypes presenting optic atrophy as a major feature.To define the relative contribution of POLG1, POLG2, ANT1 and PEO1 genes to the mtDNA multiple deletion syndromes, we analysed them in a cohort of 67 probands showing accumulation of multiple mtDNA deletions in muscle.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP751331.RAs6hNj33ToYqCn-Zk-CQXZCS_uh3cKMi1P2OokNcZk-o130_provenance.
• NP308759.RAIYVmbiFjsigr8K_p_Nmnd7dwnSeJjh371_rEgrCHoQE130_assertion description "[Finally OPA1 missense mutations are involved in phenotypes presenting optic atrophy as a major feature.To define the relative contribution of POLG1, POLG2, ANT1 and PEO1 genes to the mtDNA multiple deletion syndromes, we analysed them in a cohort of 67 probands showing accumulation of multiple mtDNA deletions in muscle.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP308759.RAIYVmbiFjsigr8K_p_Nmnd7dwnSeJjh371_rEgrCHoQE130_provenance.
• assertion description "[Finally OPA1 missense mutations are involved in phenotypes presenting optic atrophy as a major feature.To define the relative contribution of POLG1, POLG2, ANT1 and PEO1 genes to the mtDNA multiple deletion syndromes, we analysed them in a cohort of 67 probands showing accumulation of multiple mtDNA deletions in muscle.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Finally OPA1 missense mutations are involved in phenotypes presenting optic atrophy as a major feature.To define the relative contribution of POLG1, POLG2, ANT1 and PEO1 genes to the mtDNA multiple deletion syndromes, we analysed them in a cohort of 67 probands showing accumulation of multiple mtDNA deletions in muscle.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Finally OPA1 missense mutations are involved in phenotypes presenting optic atrophy as a major feature.To define the relative contribution of POLG1, POLG2, ANT1 and PEO1 genes to the mtDNA multiple deletion syndromes, we analysed them in a cohort of 67 probands showing accumulation of multiple mtDNA deletions in muscle.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP823386.RAMdy7HJOMbtkczluk9XCUHkvltxzEqZAO-_jZV9QpFgo130_assertion description "[Finally OPA1 missense mutations are involved in phenotypes presenting optic atrophy as a major feature.To define the relative contribution of POLG1, POLG2, ANT1 and PEO1 genes to the mtDNA multiple deletion syndromes, we analysed them in a cohort of 67 probands showing accumulation of multiple mtDNA deletions in muscle.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP823386.RAMdy7HJOMbtkczluk9XCUHkvltxzEqZAO-_jZV9QpFgo130_provenance.
• NP678474.RAei02ujcZ3bV5b72OXDpW5aKDR2ouBiIcwNlliJlPZoI130_assertion description "[Finally OPA1 missense mutations are involved in phenotypes presenting optic atrophy as a major feature.To define the relative contribution of POLG1, POLG2, ANT1 and PEO1 genes to the mtDNA multiple deletion syndromes, we analysed them in a cohort of 67 probands showing accumulation of multiple mtDNA deletions in muscle.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP678474.RAei02ujcZ3bV5b72OXDpW5aKDR2ouBiIcwNlliJlPZoI130_provenance.
• NP678471.RAgtHgu7i6yJFH-zb5Zjwy3O_TWuyKJkKH2BV_zy_jlsg130_assertion description "[Finally OPA1 missense mutations are involved in phenotypes presenting optic atrophy as a major feature.To define the relative contribution of POLG1, POLG2, ANT1 and PEO1 genes to the mtDNA multiple deletion syndromes, we analysed them in a cohort of 67 probands showing accumulation of multiple mtDNA deletions in muscle.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP678471.RAgtHgu7i6yJFH-zb5Zjwy3O_TWuyKJkKH2BV_zy_jlsg130_provenance.
• NP678473.RAgphk0hYfLxrjsXl_J1KdSI_kTWT4wPKo0-Nd5bYwzd0130_assertion description "[Finally OPA1 missense mutations are involved in phenotypes presenting optic atrophy as a major feature.To define the relative contribution of POLG1, POLG2, ANT1 and PEO1 genes to the mtDNA multiple deletion syndromes, we analysed them in a cohort of 67 probands showing accumulation of multiple mtDNA deletions in muscle.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP678473.RAgphk0hYfLxrjsXl_J1KdSI_kTWT4wPKo0-Nd5bYwzd0130_provenance.
• NP678475.RAp9DYVEgXWRktxGJ6x1FKQsoKDIfg1cm8fxisWKfhr-g130_assertion description "[Finally OPA1 missense mutations are involved in phenotypes presenting optic atrophy as a major feature.To define the relative contribution of POLG1, POLG2, ANT1 and PEO1 genes to the mtDNA multiple deletion syndromes, we analysed them in a cohort of 67 probands showing accumulation of multiple mtDNA deletions in muscle.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP678475.RAp9DYVEgXWRktxGJ6x1FKQsoKDIfg1cm8fxisWKfhr-g130_provenance.
• NP633486.RALpTLLeBYcv6FlxLBgqWCTBUM_zhsCqoaasjAUKiOysE130_assertion description "[Finally OPA1 missense mutations are involved in phenotypes presenting optic atrophy as a major feature.To define the relative contribution of POLG1, POLG2, ANT1 and PEO1 genes to the mtDNA multiple deletion syndromes, we analysed them in a cohort of 67 probands showing accumulation of multiple mtDNA deletions in muscle.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP633486.RALpTLLeBYcv6FlxLBgqWCTBUM_zhsCqoaasjAUKiOysE130_provenance.
• NP923813.RA8RMkGQWFdkWbO0KcmECbNhe4zI09C9B-aP__uzP15UY130_assertion description "[Finally OPA1 missense mutations are involved in phenotypes presenting optic atrophy as a major feature.To define the relative contribution of POLG1, POLG2, ANT1 and PEO1 genes to the mtDNA multiple deletion syndromes, we analysed them in a cohort of 67 probands showing accumulation of multiple mtDNA deletions in muscle.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP923813.RA8RMkGQWFdkWbO0KcmECbNhe4zI09C9B-aP__uzP15UY130_provenance.