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Volumn 46, Issue D1, 2018, Pages D1039-D1048

VarCards: An integrated genetic and clinical database for coding variants in the human genome

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTISM; CLINICAL DATA REPOSITORY; COMPUTER MODEL; FRAMESHIFT MUTATION; GENE DELETION; GENE FREQUENCY; GENE INSERTION; GENE INTERACTION; GENETIC ALGORITHM; GENETIC CODE; GENETIC DATABASE; GENETIC VARIABILITY; GENOME; GENOMICS; HUMAN; INTERNET; MAJOR CLINICAL STUDY; MISSENSE MUTATION; ONLINE SYSTEM; PRIORITY JOURNAL; RNA SPLICE SITE; SINGLE NUCLEOTIDE POLYMORPHISM; SOFTWARE; COMPUTER INTERFACE; GENETIC VARIATION; GENETICS; HUMAN GENOME; MUTATION; NUCLEIC ACID DATABASE; PHENOTYPE;

EID: 85040860512     PISSN: 03051048     EISSN: 13624962     Source Type: Journal    
DOI: 10.1093/nar/gkx1039     Document Type: Article
Times cited : (155)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.