| Literature DB >> 29221463 |
Abdulaziz Alsemari1,2, Banan Al-Younes3,2, Ewa Goljan3,2, Dyala Jaroudi3,2, Faisal BinHumaid3,2, Brian F Meyer3,2, Stefan T Arold4, Dorota Monies5,6.
Abstract
CORRECTION: After publication of the article [1], it has been brought to our attention that there is a nomenclature issue with this article. At the time of acceptance, the VARS2 mutation was considered equivalent to the VARS2 mutation. However, this has changed so that VARS now only refers to shorter mitochondrial sequence of valyl-tRNA synthesase containing 1093 amino acids. "Therefore, in the context of this article, every usage of "VARS2" should be replaced with "VARS" when referring to the causative variant".Entities:
Year: 2017 PMID: 29221463 PMCID: PMC5723066 DOI: 10.1186/s40246-017-0130-6
Source DB: PubMed Journal: Hum Genomics ISSN: 1473-9542 Impact factor: 4.639