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The muscle protein dysferlin accumulates in the Alzheimer brain

Dysferlin is a transmembrane protein that is highly expressed in muscle. Dysferlin mutations cause limb-girdle dystrophy type 2B, Miyoshi myopathy and distal anterior compartment myopathy. Dysferlin has also been described in neural tissue. We studied dysferlin distribution in the brains of patients...

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Detalles Bibliográficos
Autores principales: Galvin, James E., Palamand, Divya, Strider, Jeff, Milone, Margherita, Pestronk, Alan
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1705477/
https://www.ncbi.nlm.nih.gov/pubmed/17024495
http://dx.doi.org/10.1007/s00401-006-0147-8