Expression of BRI2 mRNA and protein in normal human brain and familial British dementia: its relevance to the pathogenesis of disease

INTRODUCTION: Two different disease-specific mutations in the BRI2 gene, situated on chromosome 13, have been identified as giving rise to familial British dementia (FBD) and familial Danish dementia (FDD). Each mutation results in extension of the open reading frame generating the disease-specific...

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Main Authors: Lashley, T., Revesz, T., Plant, G., Bandopadhyay, R., Lees, A. J., Frangione, B., Wood, N. W., de Silva, R., Ghiso, J., Rostagno, A., Holton, J. L.
Formato: Artigo
Idioma:Inglês
Publicado em: 2008
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2795351/
https://ncbi.nlm.nih.gov/pubmed/18282158
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1365-2990.2008.00935.x
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