Global Gene Profiling of VCP‐associated Inclusion Body Myopathy

Inclusion body myopathy associated with Paget’s disease of bone and frontotemporal dementia (IBMPFD) is an autosomal dominant disorder caused by mutations in the Valosin‐containing protein (VCP) gene on chromosome 9p12–13. Patients demonstrate limb girdle muscle weakness, which eventually progresses...

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Detalhes bibliográficos
Main Authors: Nalbandian, Angèle, Ghimbovschi, Svetlana, Radom‐Aizik, Shlomit, Dec, Eric, Vesa, Jouni, Martin, Barbara, Knoblach, Susan, Smith, Charles, Hoffman, Eric, Kimonis, Virginia E.
Formato: Artigo
Idioma:Inglês
Publicado em: Blackwell Publishing Inc 2012
Assuntos:
Research Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3375869/
https://ncbi.nlm.nih.gov/pubmed/22686199
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1752-8062.2012.00407.x
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