Cargando…
Characterization of CADASIL among the Han Chinese in Taiwan: Distinct Genotypic and Phenotypic Profiles
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is originally featured with a strong clustering of mutations in NOTCH3 exons 3–6 and leukoencephalopathy with frequent anterior temporal pole involvement. The present study aims at characterizing the...
Autores principales: | Liao, Yi-Chu, Hsiao, Cheng-Tsung, Fuh, Jong-Ling, Chern, Chang-Ming, Lee, Wei-Ju, Guo, Yuh-Cherng, Wang, Shuu-Jiun, Lee, I-Hui, Liu, Yo-Tsen, Wang, Yen-Feng, Chang, Feng-Chi, Chang, Ming-Hung, Soong, Bing-Wen, Lee, Yi-Chung |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4550240/ https://www.ncbi.nlm.nih.gov/pubmed/26308724 http://dx.doi.org/10.1371/journal.pone.0136501 |
Ejemplares similares
-
SORL1 gene, plasma biomarkers, and the risk of Alzheimer’s disease for the Han Chinese population in Taiwan
por: Chou, Cheng-Ta, et al.
Publicado: (2016) -
Association between Alzheimer’s disease genes and trajectories of cognitive function decline in Han Chinese in Taiwan
por: Hsieh, Tsung-Jen, et al.
Publicado: (2021) -
Validation of NINDS-VCI Neuropsychology Protocols for Vascular Cognitive Impairment in Taiwan
por: Lin, Hsiu-Fen, et al.
Publicado: (2016) -
Genome-wide analyses identify novel risk loci for cluster headache in Han Chinese residing in Taiwan
por: Chen, Shih-Pin, et al.
Publicado: (2022) -
Clinical and genetic profiles of hereditary transthyretin amyloidosis in Taiwan
por: Chao, Hua‐Chuan, et al.
Publicado: (2019)