Mosaicism for dominant collagen 6 mutations as a cause for intrafamilial phenotypic variability. (2015)

First Author: Donkervoort S

Attributed to: MICA: MRC Centre for Neuromuscular Diseases funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1002/humu.22691

PubMed Identifier: 25204870

Publication URI: http://europepmc.org/abstract/MED/25204870

Type: Journal Article/Review

Volume: 36

Parent Publication: Human mutation

Issue: 1

ISSN: 1059-7794