Joubert syndrome 13 (Q32145609)
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Joubert syndrome that has material basis in homozygous or compound heterozygous mutation in the TCTN1 gene on chromosome 12q24
- JBTS13
- JOUBERT SYNDROME 13; JBTS13
- JOUBERT SYNDROME 13
- Joubert syndrome type 13
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Joubert syndrome 13 |
Joubert syndrome that has material basis in homozygous or compound heterozygous mutation in the TCTN1 gene on chromosome 12q24 |
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Statements
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Identifiers
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1 reference