Predictive role of heterozygous p.R4810K of RNF213 in the phenotype of Chinese moyamoya disease

OBJECTIVE: Precise genetic analyses were conducted with ring finger protein 213 (RNF213) in relation to a particular clinical phenotype in Chinese patients with moyamoya disease (MMD) to determine whether heterozygosity is responsible for the early-onset and severe form of this disease. METHODS: A c...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Neurology
Main Authors: Wang, Yue, Zhang, Zhengshan, Wei, Ling, Zhang, Qian, Zou, Zhengxing, Yang, Luping, Li, Desheng, Shang, Mengke, Han, Cong, Mambiya, Michael, Li, Qian, Hao, Fangbin, Zhang, Kaili, Wang, Hui, Liu, Shan, Liu, Mengwei, Zeng, Fanxin, Nie, Fangfang, Wang, Kai, Liu, Wanyang, Duan, Lian
Formato: Artigo
Idioma:Inglês
Publicado em: Lippincott Williams & Wilkins 2020
Assuntos:
Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7176299/
https://ncbi.nlm.nih.gov/pubmed/31949090
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0000000000008901
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados