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