Cargando…
Rare variants of RNF213 and moyamoya/non-moyamoya intracranial artery stenosis/occlusion disease risk: a meta-analysis and systematic review
BACKGROUND: The p.R4810K and other rare variants of ring finger protein 213 gene (RNF213) were illustrated as susceptibility variants for moyamoya (MMD) and non-moyamoya intracranial artery stenosis/occlusion disease (ICASO) recently. However, the effect sizes of p.R4810K were in great discrepancy e...
Autores principales: | Liao, Xin, Deng, Jing, Dai, Wenjie, Zhang, Tong, Yan, Junxia |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5667490/ https://www.ncbi.nlm.nih.gov/pubmed/29165161 http://dx.doi.org/10.1186/s12199-017-0680-1 |
Ejemplares similares
-
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) -
Rare RNF213 variant in adolescent with moyamoya disease
por: Cardoso, Ivana, et al.
Publicado: (2023) -
Rare RNF213 variants and the risk of intracranial artery stenosis/occlusion disease in Chinese population: a case-control study
por: Liao, Xin, et al.
Publicado: (2019) -
RNF213 Rare Variants in Slovakian and Czech Moyamoya Disease Patients
por: Kobayashi, Hatasu, et al.
Publicado: (2016) -
Frequency and significance of rare RNF213 variants in patients with adult moyamoya disease
por: Jang, Mi-Ae, et al.
Publicado: (2017)