Long-term survival of neonatal mitochondrial complex III deficiency associated with a novel BCS1L gene mutation. (2010)

First Author: Tuppen HA

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ymgme.2010.04.010

PubMed Identifier: 20472482

Publication URI: http://europepmc.org/abstract/MED/20472482

Type: Journal Article/Review

Volume: 100

Parent Publication: Molecular genetics and metabolism

Issue: 4

ISSN: 1096-7192