Matches in Nanopublications for { ?s ?p "[Recessive mutations in the mitochondrial arginyl-transfer RNA synthetase (RARS2) gene have been associated with early onset encephalopathy with signs of oxidative phosphorylation defects classified as pontocerebellar hypoplasia 6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP326878.RAvlKFbGUF8xZmPmmCrlJW64ik9wylnrVrrYFag4IbKxE130_assertion description "[Recessive mutations in the mitochondrial arginyl-transfer RNA synthetase (RARS2) gene have been associated with early onset encephalopathy with signs of oxidative phosphorylation defects classified as pontocerebellar hypoplasia 6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP326878.RAvlKFbGUF8xZmPmmCrlJW64ik9wylnrVrrYFag4IbKxE130_provenance.
- NP615052.RAgj1EwJ4HGha8P76PElCtJxn0zgVX-s7Fk_Ygeczei_w130_assertion description "[Recessive mutations in the mitochondrial arginyl-transfer RNA synthetase (RARS2) gene have been associated with early onset encephalopathy with signs of oxidative phosphorylation defects classified as pontocerebellar hypoplasia 6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615052.RAgj1EwJ4HGha8P76PElCtJxn0zgVX-s7Fk_Ygeczei_w130_provenance.
- NP980588.RAdJaCpO1ZbFU825Wqjjz-tYa0yviuG-_dGfdrrrt_UXA130_assertion description "[Recessive mutations in the mitochondrial arginyl-transfer RNA synthetase (RARS2) gene have been associated with early onset encephalopathy with signs of oxidative phosphorylation defects classified as pontocerebellar hypoplasia 6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP980588.RAdJaCpO1ZbFU825Wqjjz-tYa0yviuG-_dGfdrrrt_UXA130_provenance.
- NP927399.RAsxNVgvL9oL8-O9PG_k6LMQB7RXWNSCzIXXv8X_Jozwo130_assertion description "[Recessive mutations in the mitochondrial arginyl-transfer RNA synthetase (RARS2) gene have been associated with early onset encephalopathy with signs of oxidative phosphorylation defects classified as pontocerebellar hypoplasia 6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP927399.RAsxNVgvL9oL8-O9PG_k6LMQB7RXWNSCzIXXv8X_Jozwo130_provenance.
- NP927413.RAme4YHQka5wd0xSFMOjuuC-hTbc0pSHeZ2mx8ICgZC5I130_assertion description "[Recessive mutations in the mitochondrial arginyl-transfer RNA synthetase (RARS2) gene have been associated with early onset encephalopathy with signs of oxidative phosphorylation defects classified as pontocerebellar hypoplasia 6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP927413.RAme4YHQka5wd0xSFMOjuuC-hTbc0pSHeZ2mx8ICgZC5I130_provenance.
- assertion description "[Recessive mutations in the mitochondrial arginyl-transfer RNA synthetase (RARS2) gene have been associated with early onset encephalopathy with signs of oxidative phosphorylation defects classified as pontocerebellar hypoplasia 6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Recessive mutations in the mitochondrial arginyl-transfer RNA synthetase (RARS2) gene have been associated with early onset encephalopathy with signs of oxidative phosphorylation defects classified as pontocerebellar hypoplasia 6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Recessive mutations in the mitochondrial arginyl-transfer RNA synthetase (RARS2) gene have been associated with early onset encephalopathy with signs of oxidative phosphorylation defects classified as pontocerebellar hypoplasia 6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Recessive mutations in the mitochondrial arginyl-transfer RNA synthetase (RARS2) gene have been associated with early onset encephalopathy with signs of oxidative phosphorylation defects classified as pontocerebellar hypoplasia 6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP980586.RAvyHA6Kyi1vtCRzeAUY2ViXWx4OfeClyYme7CtgUpulw130_assertion description "[Recessive mutations in the mitochondrial arginyl-transfer RNA synthetase (RARS2) gene have been associated with early onset encephalopathy with signs of oxidative phosphorylation defects classified as pontocerebellar hypoplasia 6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP980586.RAvyHA6Kyi1vtCRzeAUY2ViXWx4OfeClyYme7CtgUpulw130_provenance.
- NP980587.RAFeejkq7w7oGbB60DVwb8Tl8xz68-LWSfQZHN3C6JZPU130_assertion description "[Recessive mutations in the mitochondrial arginyl-transfer RNA synthetase (RARS2) gene have been associated with early onset encephalopathy with signs of oxidative phosphorylation defects classified as pontocerebellar hypoplasia 6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP980587.RAFeejkq7w7oGbB60DVwb8Tl8xz68-LWSfQZHN3C6JZPU130_provenance.
- NP927407.RA99CDRqcO9pMFejk7SxkDQc5xPQ1z8bqiP3MdEHV1Rcs130_assertion description "[Recessive mutations in the mitochondrial arginyl-transfer RNA synthetase (RARS2) gene have been associated with early onset encephalopathy with signs of oxidative phosphorylation defects classified as pontocerebellar hypoplasia 6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP927407.RA99CDRqcO9pMFejk7SxkDQc5xPQ1z8bqiP3MdEHV1Rcs130_provenance.