SMA linked to chromosome 5
Spinal muscular atrophy types 1 through 4 all result from a single known cause — a deficiency of a protein called SMN, for "survival of motor neuron."
Deficiency of SMN protein occurs when a mutation (flaw) is present in both copies of the SMN1 gene — one on each chromosome 5. Normally, most of the protein made from SMN1 genes is full-length and functional, but when mutations occur, little or no full-length, functional SMN protein is produced.