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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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| Publicado en: | Ital J Pediatr |
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| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BioMed Central
2017
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5688763/ https://ncbi.nlm.nih.gov/pubmed/29141652 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13052-017-0419-z |
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