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)
Jump to navigation
Jump to search
scientific article published on 23 October 2014
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Whole exome sequencing reveals mutations in NARS2 and PARS2, encoding the mitochondrial asparaginyl-tRNA synthetase and prolyl-tRNA synthetase, in patients with Alpers syndrome |
scientific article published on 23 October 2014 |
Statements
1 reference
Whole exome sequencing reveals mutations in NARS2 and PARS2, encoding the mitochondrial asparaginyl-tRNA synthetase and prolyl-tRNA synthetase, in patients with Alpers syndrome (English)
1 reference
Kalliopi Sofou
1 reference
Gittan Kollberg
1 reference
Maria Holmström
1 reference
Marcela Dávila
1 reference
Niklas Darin
1 reference
Elisabeth Holme
1 reference
Már Tulinius
1 reference
Jorge Asin-Cayuela
1 reference
23 October 2014
1 reference
1 reference
59-68
1 reference
Identifiers
1 reference
1 reference
1 reference