Novel homozygous missense mutation in GAN associated with Charcot-Marie-Tooth disease type 2 in a large consanguineous family from Israel. (2016)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1186/s12881-016-0343-x

PubMed Identifier: 27852232

Publication URI: http://europepmc.org/abstract/MED/27852232

Type: Journal Article/Review

Volume: 17

Parent Publication: BMC medical genetics

Issue: 1

ISSN: 1471-2350