(Q32136856)
English
autosomal recessive early-onset Parkinson disease 23
early-onset Parkinson disease that has material basis in homozygous or compound heterozygous mutation in the VPS13C gene on chromosome 15q22
- autosomal recessive early-onset Parksinson disease type 23
- autosomal recessive early-onset Parkinson's disease 23
- Parkinson Disease 23, Autosomal Recessive Early-Onset
- Parkinson's disease 23
- PARK23
Statements
2 references
1 reference
Identifiers
1 reference
2 references
1 reference
1 reference