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Hereditary Inclusion Body Myopathy: A Decade of Progress
Hereditary Inclusion Body Myopathy (HIBM) is an autosomal recessive, quadriceps sparing type commonly referred to as HIBM but also termed h-IBM or Inclusion Body Myopathy 2 (IBM2). The clinical manifestations begin with muscle weakness progressing over the next 10–20 years uniquely sparing the quadr...
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2009
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2748147/ https://ncbi.nlm.nih.gov/pubmed/19596068 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bbadis.2009.07.001 |
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