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.
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P2860
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.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
@zh-hant
name
Identification of a Novel Dele ...... ion in the Chinese Population.
@en
Identification of a Novel Deletion Mutation
@nl
type
label
Identification of a Novel Dele ...... ion in the Chinese Population.
@en
Identification of a Novel Deletion Mutation
@nl
prefLabel
Identification of a Novel Dele ...... ion in the Chinese Population.
@en
Identification of a Novel Deletion Mutation
@nl
P2093
P2860
P1476
Identification of a Novel Dele ...... ion in the Chinese Population.
@en
P2093
P2860
P2888
P356
10.1007/S12031-016-0836-2
P577
2016-09-20T00:00:00Z