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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: 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.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2003
Pynciau:
Article
Mynediad Ar-lein: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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