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Sarcoglycanopathies: molecular pathogenesis and therapeutic prospects
Sarcoglycanopathies are a group of autosomal recessive muscle-wasting disorders caused by genetic defects in one of four cell membrane glycoproteins, α-, β-, γ- or δ-sarcoglycan. These four sarcoglycans form a subcomplex that is closely linked to the major dystrophin-associated protein complex, whic...
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| Hlavní autoři: | , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Cambridge University Press
2009
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| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3279956/ https://ncbi.nlm.nih.gov/pubmed/19781108 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1017/S1462399409001203 |
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