A recurrent mitochondrial p.Trp22Arg NDUFB3 variant causes a distinctive facial appearance, short stature and a mild biochemical and clinical phenotype. (2016)

First Author: Alston CL


No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1136/jmedgenet-2015-103576

PubMed Identifier: 27091925

Publication URI: http://europepmc.org/abstract/MED/27091925

Type: Journal Article/Review

Volume: 53

Parent Publication: Journal of medical genetics

Issue: 9

ISSN: 0022-2593