Human genes for adult spinal muscular atrophy
Adult spinal muscular atrophy [DOID:0050529]
A spinal muscular atrophy that is characterized by progressive muscular weakness and motor disability that typically presents in the third decade of life and has_material_basis_in mutations in the SMN1 or SMN2 genes that are required for the survival of motor neurons.
Synonyms: adult spinal muscular atrophy, adult spinal muscular atrophies, DOID:0050529, SMA4, spinal muscular atrophy 4 ...
Linkouts: OMIM