The Homozygote VCP(R155H/R155H) Mouse Model Exhibits Accelerated Human VCP-Associated Disease Pathology

Valosin containing protein (VCP) mutations are the cause of hereditary inclusion body myopathy, Paget's disease of bone, frontotemporal dementia (IBMPFD). VCP gene mutations have also been linked to 2% of isolated familial amyotrophic lateral sclerosis (ALS). VCP is at the intersection of disru...

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Bibliografski detalji
Glavni autori: Nalbandian, Angèle, Llewellyn, Katrina J., Kitazawa, Masashi, Yin, Hong Z., Badadani, Mallikarjun, Khanlou, Negar, Edwards, Robert, Nguyen, Christopher, Mukherjee, Jogeshwar, Mozaffar, Tahseen, Watts, Giles, Weiss, John, Kimonis, Virginia E.
Format: Artigo
Jezik:Inglês
Izdano: Public Library of Science 2012
Teme:
Research Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3460820/
https://ncbi.nlm.nih.gov/pubmed/23029473
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0046308
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