(Q32142578)
English
hereditary spastic paraplegia 12
hereditary spastic paraplegia that has material basis in mutation in the RTN2 gene on chromosome 19q13
- autosomal dominant spastic paraplegia 12
- SPG12
- autosomal dominant spastic paraplegia type 12
- SPASTIC PARAPLEGIA 12, AUTOSOMAL DOMINANT; SPG12
- SPASTIC PARAPLEGIA 12, AUTOSOMAL DOMINANT
- hereditary spastic paraplegia type 12
Statements
1 reference
1 reference
1 reference
1 reference
Identifiers
1 reference
1 reference
1 reference
2 references
1 reference
1 reference
1 reference