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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Counseling and PDCD10[original query]
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.
Journal of molecular neuroscience : MN 2017 Jan 61 (1): 8-15.
Yang Chenlong, Zhao Jizong, Wu Bingquan, Zhong Haohao, Li Yan, Xu Yul
Genetic Screening of Pediatric Cavernous Malformations.
Journal of molecular neuroscience : MN 2016 Oct 60 (2): 232-8.
Merello Elisa, Pavanello Marco, Consales Alessandro, Mascelli Samantha, Raso Alessandro, Accogli Andrea, Cama Armando, Valeria Capra, De Marco Patriz
Identification of a Novel CCM1 Frameshift Mutation in a Chinese Han Family With Multiple Cerebral Cavernous Malformations.
Frontiers in neuroscience 2020 10 14 525986.
Zhang Fan, Xue Yiteng, Zhang Feng, Wei Xiaoming, Zhou Zhisong, Ma Zhaoru, Wang Xiaosong, Shen Hong, Li Yujun, Cui Xiaoying, Liu
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