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The SCN1A Mutation Database: Updating Information and Analysis of the Relationships among Genotype, Functional Alteration, and Phenotype
Meng, Heng[1,2,3,4]; Xu, Hai-Qing[1,2,3]; Yu, Lu[1,2,3]; Lin, Guo-Wang[1,2,3]; He, Na[1,2,3]; Su, Tao[1,2,3]; Shi, Yi-Wu[1,2,3]; Li, Bin[1,2,3]; Wang, Jie[1,2,3]; Liu, Xiao-Rong[1,2,3]
2015
卷号36期号:[db:dc_citation_issue]页码:573
DOI[db:dc_identifier_doi]
URL标识查看原文
WOS记录号[DB:DC_IDENTIFIER_WOSID]
内容类型期刊论文
URI标识http://www.corc.org.cn/handle/1471x/3326186
专题暨南大学
作者单位1.[1]Guangzhou Med Univ, Key Lab Neurogenet & Channelopathies Guangdong Pr, Inst Neurosci, Guangzhou 510260, Guangdong, Peoples R China
2.[2]Guangzhou Med Univ, Key Lab Neurogenet & Channelopathies Guangdong Pr, Affiliated Hosp 2, Guangzhou 510260, Guangdong, Peoples R China
3.[3]Minist Educ China, Guangzhou, Guangdong, Peoples R China
4.[4]Jinan Univ, Affiliated Hosp 1, Dept Neurol, Guangzhou, Guangdong, Peoples R China
推荐引用方式
GB/T 7714
Meng, Heng[1,2,3,4],Xu, Hai-Qing[1,2,3],Yu, Lu[1,2,3],et al. The SCN1A Mutation Database: Updating Information and Analysis of the Relationships among Genotype, Functional Alteration, and Phenotype[J],2015,36([db:dc_citation_issue]):573.
APA Meng, Heng[1,2,3,4].,Xu, Hai-Qing[1,2,3].,Yu, Lu[1,2,3].,Lin, Guo-Wang[1,2,3].,He, Na[1,2,3].,...&Liao, Wei-Ping[1,2,3].(2015).The SCN1A Mutation Database: Updating Information and Analysis of the Relationships among Genotype, Functional Alteration, and Phenotype.,36([db:dc_citation_issue]),573.
MLA Meng, Heng[1,2,3,4],et al."The SCN1A Mutation Database: Updating Information and Analysis of the Relationships among Genotype, Functional Alteration, and Phenotype".36.[db:dc_citation_issue](2015):573.
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