队列
医学
先证者
外显子组测序
外显子组
烟雾病
遗传学
生物信息学
儿科
内科学
生物
突变
基因
作者
Adam J. Kundishora,Samuel T. Peters,Amélie Pinard,Daniel Durán,Shreyas Panchagnula,Tanyeri Barak,Danielle Miyagishima,Weilai Dong,Hannah Smith,Jack Ocken,Ashley Dunbar,Carol Nelson‐Williams,Shozeb Haider,Rebecca L. Walker,Boyang Li,Hongyu Zhao,Dean Thumkeo,Arnaud Marlier,Phan Q. Duy,Nicholas S. Diab
出处
期刊:JAMA Neurology
[American Medical Association]
日期:2021-06-14
卷期号:78 (8): 993-993
被引量:48
标识
DOI:10.1001/jamaneurol.2021.1681
摘要
These findings provide the largest collection to date of non-East Asian individuals with sporadic MMD harboring pathogenic variants in the same gene. The results suggest that DIAPH1 is a novel MMD risk gene and impaired vascular cell actin remodeling in MMD pathogenesis, with diagnostic and therapeutic ramifications.
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