A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency. (2015)

First Author: Alston CL

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1007/s00439-015-1568-z

PubMed Identifier: 26008905

Publication URI: http://europepmc.org/abstract/MED/26008905

Type: Journal Article/Review

Volume: 134

Parent Publication: Human genetics

Issue: 8

ISSN: 0340-6717