Human genes for Joubert syndrome 15
Joubert syndrome 15 [DOID:0110984]
A Joubert syndrome characterized by ataxia, hypotonia, delayed psychomotor development, and variable mental retardation that has_material_basis_in homozygous mutation in the CEP41 gene on chromosome 7q32.
Synonyms: Joubert syndrome 15, DOID:0110984, JBTS15