Identification of a novel ARL13B variant in a Joubert syndrome-affected patient with retinal impairment and obesity. (2015)

First Author: Thomas S
Attributed to:  MRC Wellcome Trust Human Developmental Biology Resource (HDBR) funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/ejhg.2014.156

PubMed Identifier: 25138100

Publication URI: http://europepmc.org/abstract/MED/25138100

Type: Journal Article/Review

Volume: 23

Parent Publication: European journal of human genetics : EJHG

Issue: 5

ISSN: 1018-4813