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ARL3 Mutations Cause Joubert Syndrome by Disrupting Ciliary Protein Composition. (2018)

First Author: Alkanderi S

Attributed to: Models, modifiers and novel treatments of Joubert syndrome funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2018.08.015

PubMed Identifier: 30269812

Publication URI: http://europepmc.org/abstract/MED/30269812

Type: Journal Article/Review

Volume: 103

Parent Publication: American journal of human genetics

Issue: 4

ISSN: 0002-9297