Identification of a Novel Deletion Mutation (c.1780delG) and a Novel Splice-Site Mutation (c.1412-1G>A) in the CCM1/KRIT1 Gene Associated with Familial Cerebral Cavernous Malformation in the Chinese Population
Crossref DOI link: https://doi.org/10.1007/s12031-016-0836-2
Published Online: 2016-09-20
Published Print: 2017-01
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Yang, Chenlong
Zhao, Jizong
Wu, Bingquan
Zhong, Haohao
Li, Yan
Xu, Yulun
Funding for this research was provided by:
Beijing Municipal Natural Science Foundation (CN) (7132068)
License valid from 2016-09-20