Novel Tau Polymorphisms, Tau Haplotypes, and Splicing in Familial and Sporadic Frontotemporal Dementia

BACKGROUND: A subset of familial cases (FTDP-17) of frontotemporal dementia (FTD) are caused by mutations in the tau gene. The role of tau gene mutations and haplotypes in sporadic FTD and the functional consequences of tau polymorphisms are unknown. OBJECTIVES: To investigate (1) the frequency of k...

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Detalhes bibliográficos
Main Authors: Sobrido, Maria-Jesús, Miller, Bruce L., Havlioglu, Necat, Zhukareva, Victoria, Jiang, Zhihong, Nasreddine, Ziad S., Lee, Virginia M.-Y., Chow, Tiffany W., Wilhelmsen, Kirk C., Cummings, Jeffrey L., Wu, Jane Y., Geschwind, Daniel H.
Formato: Artigo
Idioma:Inglês
Publicado em: 2003
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2072863/
https://ncbi.nlm.nih.gov/pubmed/12756133
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/archneur.60.5.698
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