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δ-Sarcoglycan-deficient muscular dystrophy: from discovery to therapeutic approaches
Mutations in the δ-sarcoglycan gene cause limb-girdle muscular dystrophy 2F (LGMD2F), an autosomal recessive disease that causes progressive weakness and wasting of the proximal limb muscles and often has cardiac involvement. Here we review the clinical implications of LGMD2F and discuss the current...
Tallennettuna:
| Päätekijät: | , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2011
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3156636/ https://ncbi.nlm.nih.gov/pubmed/21798091 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/2044-5040-1-13 |
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