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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Bibliografski detalji
Glavni autori: Nalbandian, Angèle, Ghimbovschi, Svetlana, Radom‐Aizik, Shlomit, Dec, Eric, Vesa, Jouni, Martin, Barbara, Knoblach, Susan, Smith, Charles, Hoffman, Eric, Kimonis, Virginia E.
Format: Artigo
Jezik:Inglês
Izdano: Blackwell Publishing Inc 2012
Teme:
Research Articles
Online pristup: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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