Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype. (2016)

First Author: Alston CL

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2016.05.021

PubMed Identifier: 27374774

Publication URI: http://europepmc.org/abstract/MED/27374774

Type: Journal Article/Review

Volume: 99

Parent Publication: American journal of human genetics

Issue: 1

ISSN: 0002-9297