Related references
Note: Only part of the references are listed.OFD1 Is Mutated in X-Linked Joubert Syndrome and Interacts with LCA5-Encoded Lebercilin
Karlien L. M. Coene et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2009)
Joubert Syndrome: Insights Into Brain Development, Cilium Biology, and Complex Disease
Dan Doherty
SEMINARS IN PEDIATRIC NEUROLOGY (2009)
CC2D2A, encoding a coiled-coil and C2 domain protein, causes autosomal-recessive mental retardation with retinitis pigmentosa
Abdul Noor et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Genotypes and phenotypes of Joubert syndrome and related disorders
Enza Maria Valente et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2008)