Mutation spectrum in RAB3GAP1, RAB3GAP2, and RAB18 and genotype-phenotype correlations in warburg micro syndrome and Martsolf syndrome. (2013)

First Author: Handley MT
Attributed to:  Genetic models of human disease funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1002/humu.22296

PubMed Identifier: 23420520

Publication URI: http://europepmc.org/abstract/MED/23420520

Type: Journal Article/Review

Volume: 34

Parent Publication: Human mutation

Issue: 5

ISSN: 1059-7794