6-minute walk test as a measure of disease progression and fatigability in a cohort of individuals with RYR1-related myopathies

BACKGROUND: RYR1-related Myopathies (RYR1-RM) comprise a group of rare neuromuscular diseases (NMDs) occurring in approximately 1/90000 people in the US pediatric population. RYR1-RM result from pathogenic mutations in the ryanodine receptor isoform-1 (RYR1) gene where consequent RyR1 protein calciu...

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Detalles Bibliográficos
Autores principales: Witherspoon, Jessica W., Vasavada, Ruhi P., Waite, Melissa R., Shelton, Monique, Chrismer, Irene C., Wakim, Paul G., Jain, Minal S., Bönnemann, Carsten G., Meilleur, Katherine G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6029052/
https://www.ncbi.nlm.nih.gov/pubmed/29970108
http://dx.doi.org/10.1186/s13023-018-0848-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6029052/
https://www.ncbi.nlm.nih.gov/pubmed/29970108
http://dx.doi.org/10.1186/s13023-018-0848-9

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