(Q32143240)
English
hereditary spastic paraplegia 6
A hereditary spastic paraplegia that is usually characterized by rapidly progressive and severe spastic paraplegia and has material basis in mutation in the NIPA1 gene on chromosome 15q11.2
- autosomal dominant familial spastic paraplegia type 3
- FSP3
- SPG6
- autosomal dominant spastic paraplegia type 6
- autosomal dominant spastic paraplegia 6
- Familial Spastic Paraplegia, Autosomal Dominant, 3
- SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT; SPG6
- hereditary spastic paraplegia type 6
- SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT
Statements
1 reference
1 reference
1 reference
4 references
1 reference
Identifiers
1 reference
1 reference
2 references
1 reference
1 reference
1 reference
Sitelinks
Wikipedia(1 entry)
- enwiki Spastic paraplegia 6