How do SMA-linked mutations of SMN1 lead to structural/functional deficiency of the SMA protein?

Li, W

Li, W (reprint author), Shantou Univ, Med Coll, Shantou City, Guangdong, Peoples R China.

PLOS ONE, 2017; 12 (6):

Abstract

Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disease with dysfunctional alpha-motor neurons in the anterior horn of the spina......

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