(Q32143002)
English
hereditary spastic paraplegia 41
A hereditary spastic paraplegia that has material basis in variation in the chromosome region 11p14.1-p11.2.
- autosomal dominant spastic paraplegia 41
- autosomal dominant spastic paraplegia type 41
- SPG41
- SPASTIC PARAPLEGIA 41, AUTOSOMAL DOMINANT; SPG41
- SPASTIC PARAPLEGIA 41, AUTOSOMAL DOMINANT
- hereditary spastic paraplegia type 41
Statements
1 reference
1 reference
1 reference
1 reference
Identifiers
1 reference
2 references
1 reference
1 reference