Exome Sequencing Identifies LOXL2 Mutation as a Cause of Familial Intracranial Aneurysm.
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DOI: 10.1016/j.wneu.2017.10.094
Abstract: BACKGROUND Genetic risk factors can contribute to the etiology of intracranial aneurysms (IAs), and the genetic predisposition of IAs is largely unknown. Our study aimed to explore the role of rare variations in IA susceptibility.… read more here.
Keywords: exome sequencing; mutation cause; sequencing identifies; loxl2 mutation ... See more keywords