Whole exome sequencing reveals mutations in NARS2 and PARS2, encoding the mitochondrial asparaginyl-tRNA synthetase and prolyl-tRNA synthetase, in patients with Alpers syndrome (Q42144464)
scientific article published on 23 October 2014
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Current Data About Whole exome sequencing reveals mutations in NARS2 and PARS2, encoding the mitochondrial asparaginyl-tRNA synthetase and prolyl-tRNA synthetase, in patients with Alpers syndrome
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(P1476) "Whole exome sequencing reveals mutations in NARS2 and PARS2, encoding the mitochondrial asparaginyl-tRNA synthetase and prolyl-tRNA synthetase, in patients with Alpers syndrome" (language: en)
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Gittan Kollberg
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Maria Holmström
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Marcela Dávila
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Niklas Darin
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Elisabeth Holme
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Már Tulinius
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Jorge Asin-Cayuela
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other details
description scientific article published on 23 October 2014

External Links
(P356) 10.1002/MGG3.115
(P698) 25629079
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(P5875) 267340616