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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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.
Format: Artigo
Language:Inglês
Published: 2003
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Online Access: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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