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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| Description | scientific article published on 23 October 2014 |
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author: Claes M. Gustafsson Anders Oldfors |
| Publication date | October 23, 2014 |
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