Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome. (2008)
Attributed to:
Molecular genetics of Meckel-Gruber syndrome, and functional characterization of meckelin and MKS1
funded by
MRC
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