BRD2 and TAP-1 genes and juvenile myoclonic epilepsy

Neurological Sciences

Volumn 31, Issue 1, 2010, Pages 53-56

  Layouni, Samia ^a   Buresi, Catherine ^b   Thomas, Pierre ^c   Malafosse, Alain ^b,d,f   Dogui, Mohamed ^a,e  

^a UNIVERSITY OF MONASTIR   (Tunisia)

^b GENEVA UNIVERSITY HOSPITALS   (Switzerland)

^c UNIVERSITY HOSPITAL OF NICE   (France)

^d UNIVERSITY OF GENEVA   (Switzerland)

^e SAHLOUL UNIVERSITY HOSPITAL   (Tunisia)

^f Clinique de Belle Idee   (Switzerland)

Author keywords

Association study; BRD2; Genetics; Juvenile myoclonic epilepsy; TAP 1

Indexed keywords

MEMBRANE PROTEIN; PROTEIN BRD2; TRANSPORTER ASSOCIATED WITH ANTIGEN PROCESSING 1; UNCLASSIFIED DRUG;

ADULT; ARTICLE; CHROMOSOME 6P; CONTROLLED STUDY; FEMALE; GENE ASSIGNMENT; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; MARKER GENE; MYOCLONUS EPILEPSY; PHOTOSENSITIVE EPILEPSY; SINGLE NUCLEOTIDE POLYMORPHISM;

ADULT; ATP-BINDING CASSETTE TRANSPORTERS; FEMALE; FRANCE; GENE FREQUENCY; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HAPLOTYPES; HUMANS; MALE; MYOCLONIC EPILEPSY, JUVENILE; POLYMORPHISM, GENETIC; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEIN-SERINE-THREONINE KINASES; SEQUENCE ANALYSIS, DNA;

EID: 76449094394     PISSN: 15901874     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10072-009-0190-z     Document Type: Article

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