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Limb girdle muscular dystrophy type 2B masquerading as inflammatory myopathy: case report
Limb girdle muscular dystrophy type 2B is a rare subtype of muscular dystrophy, the predominant feature of which is muscle weakness. The disease is caused by an autosomal recessively inherited reduction/absence of muscle dysferlin due to a mutation in dysferlin gene at 2p12-14. We report a 10 year o...
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| Main Authors: | , , , , , |
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| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
BioMed Central
2013
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3652784/ https://ncbi.nlm.nih.gov/pubmed/23641709 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1546-0096-11-19 |
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