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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Hauptverfasser: 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
Sprache:Inglês
Veröffentlicht: Public Library of Science 2012
Schlagworte:
Research Article
Online Zugang: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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