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Merosin‐deficient congenital muscular dystrophy: neuropathology case reports
The aims of our study were: to present cases of congenital muscular dystrophy (CMD) with deficiency in merosin and the importance of immunohistochemistry in the diagnosis of merosin‐deficient CMD. In four years (1997‐2000), we found three patients with merosin‐deficient CMD, one of them having an un...
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| Pubblicato in: | J Cell Mol Med |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Blackwell Publishing Ltd
2007
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6745520/ https://ncbi.nlm.nih.gov/pubmed/12067464 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1582-4934.2000.tb00129.x |
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