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C9orf72 immunohistochemistry in Alzheimer's disease

Mutation in chromosome 9 open reading frame 72 (C9orf72) is a major genetic cause of frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS), referred to as C9FTD/ALS. The function of the protein is currently unknown, and the pathomechanism of C9FTD/ALS remains to be elucidated. The st...

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Detalles Bibliográficos
Autor principal:	Hortobágyi, Tibor
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2012
Materias:	Commentary
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3580394/ https://www.ncbi.nlm.nih.gov/pubmed/23014271 http://dx.doi.org/10.1186/alzrt140

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