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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Autors principals: 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.
Format: Artigo
Idioma:Inglês
Publicat: 2003
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Article
Accés en línia: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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