Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome. (2008)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2008.06.023

PubMed Identifier: 18674751

Publication URI: http://europepmc.org/abstract/MED/18674751

Type: Journal Article/Review

Volume: 83

Parent Publication: American journal of human genetics

Issue: 2

ISSN: 0002-9297