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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