(Q66084911)
English
distal hereditary motor neuronopathy type 8
human disease
- autosomal dominant benign distal spinal muscular atrophy
- HMN8
- DHMN8
- congenital benign spinal muscular atrophy with contractures
- distal hereditary motor neuropathy type VIII
- autosomal dominant congenital benign spinal muscular atrophy
- congenital nonprogressive spinal muscular atrophy
Statements
1 reference
Identifiers
1 reference
1 reference