Cargando…
Rare RNF213 variants and the risk of intracranial artery stenosis/occlusion disease in Chinese population: a case-control study
BACKGROUND: RNF213 rare variant-p.R4810K (rs112735431) was significantly associated with intracranial artery stenosis/occlusion disease (ICASO) in Japan and Korea and to a lesser degree in China. Considering the allelic heterogeneity, we performed target exome sequencing of RNF213 with the aim to id...
Autores principales: | Liao, Xin, Zhang, Tong, Li, Bingyang, Hu, Shimin, Liu, Junyu, Deng, Jing, Tan, Hongzhuan, Yan, Junxia |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6441181/ https://www.ncbi.nlm.nih.gov/pubmed/30925911 http://dx.doi.org/10.1186/s12881-019-0788-9 |
Ejemplares similares
-
Association of rare RNF213 variants and intracranial aneurysm risk in a Chinese population
por: Li, Yaqi, et al.
Publicado: (2022) -
Rare variants of RNF213 and moyamoya/non-moyamoya intracranial artery stenosis/occlusion disease risk: a meta-analysis and systematic review
por: Liao, Xin, et al.
Publicado: (2017) -
Genetic analysis of RNF213 p.R4810K variant in non-moyamoya intracranial artery stenosis/occlusion disease in a Chinese population
por: Zhang, Tong, et al.
Publicado: (2017) -
Distribution of Intracranial Major Artery Stenosis/Occlusion According to RNF213 Polymorphisms
por: Kim, Jinkwon, et al.
Publicado: (2020) -
Comprehensive investigation of RNF213 nonsynonymous variants associated with intracranial artery stenosis
por: Hongo, Hiroki, et al.
Publicado: (2020)