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Volumn 53, Issue 2, 2012, Pages 308-318

Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies

(130)  Leu, Costin a,b   de Kovel, Carolien c   Zara, Federico a,d,ap   Striano, Salvatore aq   Pezzella, Marianna a,d,ap   Robbiano, Angela a,d,ap   Bianchi, Amedeo a,e,aq   Bisulli, Francesca a,f,aq   Coppola, Antonietta a,g,aq   Giallonardo, Anna Teresa a,h,aq   Beccaria, Francesca a,i,aq   Trenité, Dorothée Kasteleijn Nolst a,c   Lindhout, Dick a,c,j   Gaus, Verena a,k   Schmitz, Bettina a,k   Janz, Dieter a,k   Weber, Yvonne l   Becker, Felicitas a,l   Lerche, Holger a,l   Kleefuß Lie, Ailing A a,m   more..


Author keywords

Absence seizure; Complex inheritance; Genetic generalized epilepsy; Linkage analysis; Myoclonic seizure

Indexed keywords

ARTICLE; CHROMOSOMAL LOCALIZATION; CLINICAL ASSESSMENT; CONTROLLED STUDY; EPILEPSY; FAMILY; GENE FREQUENCY; GENE LOCUS; GENETIC ASSOCIATION; GENETIC GENERALIZED EPILEPSY; GENETIC LINKAGE; GENETIC RISK; GENETIC SUSCEPTIBILITY; GENOTYPE PHENOTYPE CORRELATION; HUMAN; MAJOR CLINICAL STUDY; MYOCLONUS EPILEPSY; PRIORITY JOURNAL; RISK ASSESSMENT; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 84856357672     PISSN: 00139580     EISSN: 15281167     Source Type: Journal    
DOI: 10.1111/j.1528-1167.2011.03379.x     Document Type: Article
Times cited : (32)

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