Possible implication of undescribed SMN1-SMN2 genotype in chronic EMG-pattern of SMA with transitory acute denervation

Spinal muscular atrophy (SMA) refers to a group of genetic neuromuscular disorders affecting lower motor neurons causative of numerous phenotypes. To date, according to the age of onset, maximum muscular activity achieved, and life expectation four types of SMA are recognized, all caused by mutation...

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Detalles Bibliográficos
Autores principales: Vitello, Girolamo A., Calì, Francesco, Vinci, Mirella, Scuderi, Carmela, L’Episcopo, Francesca, Musumeci, Antonino, Musumeci, Sebastiano A., Nicotera, Antonio G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Society of Musculoskeletal and Neuronal Interactions 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7716687/
https://www.ncbi.nlm.nih.gov/pubmed/33265090

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7716687/
https://www.ncbi.nlm.nih.gov/pubmed/33265090

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