Human genes for Joubert syndrome 33
Joubert syndrome 33 [DOID:0080279]
A Joubert syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the PIBF1 gene on chromosome 13q21.
Synonyms: Joubert syndrome 33, DOID:0080279
Joubert syndrome 33 [DOID:0080279]
A Joubert syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the PIBF1 gene on chromosome 13q21.
Synonyms: Joubert syndrome 33, DOID:0080279