smn1

This article is about a genetic disorder associated with mutation in the SMN1 gene

spinal muscular atrophy (SMA)

is an autosomal recessive disease caused by a genetic defect in the SMN1 gene, which encodes SMN, a protein widely expressed in all eukaryotic cells.

SMN is apparently selectively necessary for survival of motor neurons, as diminished abundance of the protein results in loss of function of neuronal c...