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Identification of a Novel Deletion Mutation (c.1780delG) and a Novel Splice-Site Mutation (c.1412-1G>A) in theCCM1/KRIT1Gene Associated with Familial Cerebral Cavernous Malformation in the Chinese Population
Yang, Chenlong, Zhao, Jizong, Wu, Bingquan, Zhong, Haohao, Li, Yan, Xu, YulunVolume:
61
Language:
english
Journal:
Journal of Molecular Neuroscience
DOI:
10.1007/s12031-016-0836-2
Date:
January, 2017
File:
PDF, 1.71 MB
english, 2017