Pyramidal signs in a Caucasian patient with spinal muscular atrophy: a case report. [electronic resource]
- Folia neuropathologica 2016
- 418-421 p. digital
Publication Type: Case Reports; Journal Article
1509-572X
10.5114/fn.2016.64821 doi
Exons--genetics Gene Deletion Humans Male Motor Neurons--pathology Muscular Atrophy, Spinal--diagnosis Phenotype SMN Complex Proteins--genetics Survival of Motor Neuron 1 Protein--genetics White People Young Adult