An association analysis of reelin gene (RELN) polymorphisms with childhood epilepsy in eastern Indian population from West Bengal

Cellular and Molecular Neurobiology

Volumn 31, Issue 1, 2011, Pages 45-56

  Dutta, Shruti ^a   Gangopadhyay, Prasanta K ^b   Sinha, Swagata ^a   Chatterjee, Anindita ^a   Ghosh, Saurabh ^c   Rajamma, Usha ^a  

^a Manovikas Kendra Rehabilitation and Research Institute for the Handicapped   (India)

^b CALCUTTA NATIONAL MEDICAL COLLEGE   (India)

^c INDIAN STATISTICAL INSTITUTE   (India)

Author keywords

Case control analyses; Childhood epilepsy; Genetic association; Haplotype analysis; Linkage disequilibrium; RELN

Indexed keywords

GENOMIC DNA; REELIN;

ADOLESCENT; ADULT; ARTICLE; CHILD; CONTROLLED STUDY; EPILEPSY; EXON; FEMALE; GENE LINKAGE DISEQUILIBRIUM; GENETIC ASSOCIATION; GENETIC MARKER; GENETIC POLYMORPHISM; GENOTYPE; HAPLOTYPE; HUMAN; HUMAN CELL; INDIA; INDIAN; INTRON; LEUKOCYTE; MAJOR CLINICAL STUDY; MALE; NUCLEOTIDE SEQUENCE; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD;

ADOLESCENT; ADULT; AGE OF ONSET; CASE-CONTROL STUDIES; CELL ADHESION MOLECULES, NEURONAL; CHILD; CHILD, PRESCHOOL; EPILEPSY; EXTRACELLULAR MATRIX PROTEINS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENETICS, POPULATION; GENOME-WIDE ASSOCIATION STUDY; HUMANS; INDIA; INFANT; LINKAGE DISEQUILIBRIUM; MALE; NERVE TISSUE PROTEINS; POLYMORPHISM, SINGLE NUCLEOTIDE; SERINE ENDOPEPTIDASES; YOUNG ADULT;

EID: 79151479686     PISSN: 02724340     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10571-010-9551-7     Document Type: Article

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