Patient-Reported Prevalence of Non-motor Symptoms Is Low in Adult Patients Suffering From 5q Spinal Muscular Atrophy

Background: 5q spinal muscular atrophy (SMA) is an autosomal recessive lower motoneuron disease caused by deletion or mutations in the survival motor neuron 1 gene (SMN1) which results in reduced expression of full-length SMN protein. The main symptoms are caused by spinal motor neuron demise leadin...

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Detalhes bibliográficos
Publicado no:Front Neurol
Main Authors: Günther, René, Wurster, Claudia Diana, Cordts, Isabell, Koch, Jan Christoph, Kamm, Christoph, Petzold, Daniel, Aust, Elisa, Deschauer, Marcus, Lingor, Paul, Ludolph, Albert Christian, Hermann, Andreas
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2019
Assuntos:
Neurology
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6838202/
https://ncbi.nlm.nih.gov/pubmed/31736847
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2019.01098
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