Congenital myopathies: clinical phenotypes and new diagnostic tools

Congenital myopathies are a group of genetic muscle disorders characterized clinically by hypotonia and weakness, usually from birth, and a static or slowly progressive clinical course. Historically, congenital myopathies have been classified on the basis of major morphological features seen on musc...

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Detalles Bibliográficos
Autores principales: Cassandrini, Denise, Trovato, Rosanna, Rubegni, Anna, Lenzi, Sara, Fiorillo, Chiara, Baldacci, Jacopo, Minetti, Carlo, Astrea, Guja, Bruno, Claudio, Santorelli, Filippo M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5688763/
https://www.ncbi.nlm.nih.gov/pubmed/29141652
http://dx.doi.org/10.1186/s13052-017-0419-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5688763/
https://www.ncbi.nlm.nih.gov/pubmed/29141652
http://dx.doi.org/10.1186/s13052-017-0419-z

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