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


No abstract provided

Bibliographic Information

Digital Object Identifier:

PubMed Identifier: 23420520

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Type: Journal Article/Review

Volume: 34

Parent Publication: Human mutation

Issue: 5

ISSN: 1059-7794