Monogenic Causes in Familial Stroke Across Intracerebral Hemorrhage and Ischemic Stroke Subtypes Identified by Whole-Exome Sequencing

Whole exome sequencing (WES) has been used to detect rare causative variants in neurological diseases. However, the efficacy of WES in genetic diagnosis of clinically heterogeneous familial stroke remains inconclusive. We prospectively searched for disease-causing variants in unrelated probands with...

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Detalles Bibliográficos
Autores principales: Chang, Li-Hsin, Chi, Nai-Fang, Chen, Chun-Yu, Lin, Yung-Shuan, Hsu, Shao-Lun, Tsai, Jui-Yao, Huang, Hui-Chi, Lin, Chun-Jen, Chung, Chih-Ping, Tung, Chien-Yi, Jeng, Chung-Jiuan, Lee, Yi-Chung, Liu, Yo-Tsen, Lee, I-Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10333419/
https://www.ncbi.nlm.nih.gov/pubmed/36580209
http://dx.doi.org/10.1007/s10571-022-01315-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10333419/
https://www.ncbi.nlm.nih.gov/pubmed/36580209
http://dx.doi.org/10.1007/s10571-022-01315-3

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