Molecular genetic features and clinical manifestations in Chinese familial cerebral cavernous malformation: from a novel KRIT1/CCM1 mutation (c.1119dupT) to an overall view.

Chen, Yanming; Dong, Xuchen; Wang, Ye; Lv, Haijun; Chen, Nan; Wang, Zhongyong; Chen, Si; Chen, Ping; Xiao, Sheng; Zhao, Jizong; Dong, Jun

Chen, Yanming; Dong, Xuchen; Wang, Ye; Lv, Haijun; Chen, Nan; Wang, Zhongyong; Chen, Si; Chen, Ping; Xiao, Sheng; Zhao, Jizong; Dong, Jun.

Afiliação

Chen Y; Department of Neurosurgery, Second Affiliated Hospital of Soochow University, Suzhou, China.
Dong X; Department of Neurosurgery, Huashan Hospital, Fudan University, Shanghai, China.
Wang Y; Health Management Center, Second Affiliated Hospital of Soochow University, Suzhou, China.
Lv H; Department of Pathology, Second Affiliated Hospital of Soochow University, Suzhou, China.
Chen N; Suzhou Sano Precision Medicine Ltd., Suzhou, China.
Wang Z; Department of Neurosurgery, Second Affiliated Hospital of Soochow University, Suzhou, China.
Chen S; Suzhou Sano Precision Medicine Ltd., Suzhou, China.
Chen P; Suzhou Sano Precision Medicine Ltd., Suzhou, China.
Xiao S; Department of Pathology, Brigham and Women's Hospital, Boston, MA, United States.
Zhao J; Department of Neurosurgery, Second Affiliated Hospital of Soochow University, Suzhou, China.
Dong J; Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.