Immunoreactivity of valosin-containing protein in sporadic amyotrophic lateral sclerosis and in a case of its novel mutant

BACKGROUND: Mutations in the valosin-containing protein (VCP) gene were first found to cause inclusion- body myopathy with early-onset Paget disease and frontotemporal dementia (IBMPFD). Mutations in the VCP gene were later reported to occur in familial amyotrophic lateral sclerosis (ALS). But the r...

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Detalles Bibliográficos
Autores principales: Ayaki, Takashi, Ito, Hidefumi, Fukushima, Hiroko, Inoue, Takeshi, Kondo, Takayuki, Ikemoto, Akito, Asano, Takeshi, Shodai, Akemi, Fujita, Takuji, Fukui, Satoshi, Morino, Hiroyuki, Nakano, Satoshi, Kusaka, Hirofumi, Yamashita, Hirofumi, Ihara, Masafumi, Matsumoto, Riki, Kawamata, Jun, Urushitani, Makoto, Kawakami, Hideshi, Takahashi, Ryosuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4297454/
https://www.ncbi.nlm.nih.gov/pubmed/25492614
http://dx.doi.org/10.1186/s40478-014-0172-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4297454/
https://www.ncbi.nlm.nih.gov/pubmed/25492614
http://dx.doi.org/10.1186/s40478-014-0172-0

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