Variable expressivity of ciliopathy neurological phenotypes that encompass Meckel-Gruber syndrome and Joubert syndrome is caused by complex de-regulated ciliogenesis, Shh and Wnt signalling defects. (2013)
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/10.1093/hmg/dds546
PubMed Identifier: 23283079
Publication URI: http://europepmc.org/abstract/MED/23283079
Type: Journal Article/Review
Volume: 22
Parent Publication: Human molecular genetics
Issue: 7
ISSN: 0964-6906