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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Bibliografiset tiedot
Päätekijät: Nalbandian, Angèle, Ghimbovschi, Svetlana, Radom‐Aizik, Shlomit, Dec, Eric, Vesa, Jouni, Martin, Barbara, Knoblach, Susan, Smith, Charles, Hoffman, Eric, Kimonis, Virginia E.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Blackwell Publishing Inc 2012
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Research Articles
Linkit: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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