Identification of a Novel Variant in CC2D1A Gene Linked to Autosomal Recessive Intellectual Disability 3 in an Iranian Family and Investigating the Structure and Pleiotropic Effects of this Gene
在伊朗一个家族中鉴定出与常染色体隐性遗传智力障碍3型相关的CC2D1A基因新变异,并研究该基因的结构和多效性
期刊:Iranian Journal of Child Neurology
影响因子:0.9
doi:10.22037/ijcn.v18i1.42188
Rashvand, Zahra; Najmabadi, Hossein; Kahrizi, Kimia; Mozhdehipanah, Hossein; Moradi, Mohammad; Estaki, Zohreh; Taherkhani, Khadijeh; Nikzat, Nooshin; Najafipour, Reza; Omrani, Mir Davood