Detection of Novel Mutation in Ccm3 Causes Familial Cerebral Cavernous Malformations.
about
Exome capture sequencing identifies a novel CCM1 mutation in a Chinese family with multiple cerebral cavernous malformations.A Novel CCM1/KRIT1 Heterozygous Nonsense Mutation (c.1864C>T) Associated with Familial Cerebral Cavernous Malformation: a Genetic Insight from an 8-Year Continuous Observational Study.
P2860
Detection of Novel Mutation in Ccm3 Causes Familial Cerebral Cavernous Malformations.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年学术文章
@wuu
2015年学术文章
@zh-cn
2015年学术文章
@zh-hans
2015年学术文章
@zh-my
2015年学术文章
@zh-sg
2015年學術文章
@yue
2015年學術文章
@zh
2015年學術文章
@zh-hant
name
Detection of Novel Mutation in Ccm3 Causes Familial Cerebral Cavernous Malformations.
@en
Detection of Novel Mutation in Ccm3 Causes Familial Cerebral Cavernous Malformations.
@nl
type
label
Detection of Novel Mutation in Ccm3 Causes Familial Cerebral Cavernous Malformations.
@en
Detection of Novel Mutation in Ccm3 Causes Familial Cerebral Cavernous Malformations.
@nl
prefLabel
Detection of Novel Mutation in Ccm3 Causes Familial Cerebral Cavernous Malformations.
@en
Detection of Novel Mutation in Ccm3 Causes Familial Cerebral Cavernous Malformations.
@nl
P2093
P2860
P1476
Detection of Novel Mutation in Ccm3 Causes Familial Cerebral Cavernous Malformations
@en
P2093
Alessia Ruggeri
Antonina Sidoti
Concetta Scimone
Placido Bramanti
Zoe Katsarou
P2860
P2888
P304
P356
10.1007/S12031-015-0606-6
P577
2015-06-27T00:00:00Z