(Q32145579)
English
Joubert syndrome 1
Joubert syndrome that has material basis in homozygous mutation in the INPP5E gene on chromosome 9q34
- CORS1
- cerebelloparenchymal disorder IV
- JBTS1
- cerebellooculorenal syndrome 1
- CPD4
- Joubert syndrome type 1
- Cerebelloparenchymal Disorder 4
- Joubert-Boltshauser Syndrome
- JOUBERT SYNDROME 1
- JOUBERT SYNDROME 1; JBTS1
- Joubert Syndrome
Statements
2 references
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference