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Spinal Muscular Atrophy (SMA) Subtype Concordance in Siblings: Findings From the Cure SMA Cohort
BACKGROUND: Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disorder caused by homozygous survival of motor neuron 1 (SMN1) gene disruption. Despite a genetic etiology, little is known about subtype concordance among siblings. OBJECTIVE: To investigate subtype concordance among...
Autores principales: | Jones, Cynthia C., Cook, Suzanne F., Jarecki, Jill, Belter, Lisa, Reyna, Sandra P., Staropoli, John, Farwell, Wildon, Hobby, Kenneth |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
IOS Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7029365/ https://www.ncbi.nlm.nih.gov/pubmed/31707372 http://dx.doi.org/10.3233/JND-190399 |
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