Case report: Expanding the phenotype of ARHGEF17 mutations from increased intracranial aneurysm risk to a neurodevelopmental disease
病例报告:ARHGEF17 基因突变表型从颅内动脉瘤风险增加扩展至神经发育疾病
期刊:Frontiers in Neurology
影响因子:2.8
doi:10.3389/fneur.2022.1017654
Ravindran, Ethiraj; Ullah, Noor; Mani, Shyamala; Chew, Elaine Guo Yan; Tandiono, Moses; Foo, Jia Nee; Khor, Chiea Chuen; Kaindl, Angela M; Siddiqi, Saima