SCOPUS 정보 검색 플랫폼

Volumn 49, Issue 2, 2002, Pages 173-177

Failure to replicate an allelic association between an exon 8 polymorphism of the human α1A calcium channel gene and common syndromes of idiopathic generalized epilepsy

(5) Sander, Thomas a Toliat, Mohammad R b Heils, Armin c Becker, Christian b Nürnberg, Peter a,b

a CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN (Germany)

b MAX DELBRÜCK CENTER FOR MOLECULAR MEDICINE (Germany)

c UNIVERSITY HOSPITAL BONN (Germany)

Author keywords

Association; CACNA1A; Calcium channel; Genetics; Idiopathic generalized epilepsy

Indexed keywords

CALCIUM CHANNEL; GENOMIC DNA;

ALLELE; ARTICLE; CHILD PARENT RELATION; CONTROLLED STUDY; EXON; GENE LINKAGE DISEQUILIBRIUM; GENE REPLICATION; GENE SEQUENCE; GENERALIZED EPILEPSY; GENETIC VARIABILITY; GENOTYPE; GENOTYPE PHENOTYPE CORRELATION; HUMAN; MAJOR CLINICAL STUDY; MYOCLONUS EPILEPSY; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; VALIDATION PROCESS;

ALLELES; CALCIUM CHANNELS; DNA REPLICATION; EPILEPSY, GENERALIZED; EXONS; GENE FREQUENCY; GENOTYPE; HUMANS; POLYMORPHISM, GENETIC; PROTEIN SUBUNITS;

EID: 0036285508 PISSN: 09201211 EISSN: None Source Type: Journal
DOI: 10.1016/S0920-1211(02)00025-6 Document Type: Article

Times cited : (18)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.