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Volumn 2, Issue 9, 2015, Pages 1063-1070

Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in Epilepsy

(32)  Leu, Costin a   Balestrini, Simona a,b,c   Maher, Bridget a,b   Hernández Hernández, Laura a,b   Gormley, Padhraig d,e   Hämäläinen, Eija f   Heggeli, Kristin a   Schoeler, Natasha a   Novy, Jan g   Willis, Joseph a   Plagnol, Vincent h   Ellis, Rachael i,j   Reavey, Eleanor i,j   O'Regan, Mary i   Pickrell, William O k   Thomas, Rhys H k   Chung, Seo Kyung k   Delanty, Norman l   McMahon, Jacinta M m   Malone, Stephen n   more..


Author keywords

Association; Burden; Death; Epilepsy; Mortality; Severity

Indexed keywords

ADULT; ARTICLE; CONTROLLED STUDY; DISEASE DURATION; EPILEPSY; EXOME; FEMALE; FOLLOW UP; FUNDING; GENE FREQUENCY; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC RISK; GENETIC VARIABILITY; HUMAN; INTELLECTUAL IMPAIRMENT; MAJOR CLINICAL STUDY; MALE; MORTALITY; PHENOTYPE; PRIORITY JOURNAL; SEIZURE; SEVERE MYOCLONIC EPILEPSY IN INFANCY; SUDDEN DEATH; CAUSE OF DEATH; DNA SEQUENCE; GENETIC ASSOCIATION STUDY; GENETIC PREDISPOSITION; GENETIC VARIATION; GENETICS; GENOME-WIDE ASSOCIATION STUDY; MULTIFACTORIAL INHERITANCE; PATHOLOGY; PROCEDURES; RISK FACTOR; SEVERITY OF ILLNESS INDEX;

EID: 84953742915     PISSN: None     EISSN: 23523964     Source Type: Journal    
DOI: 10.1016/j.ebiom.2015.07.005     Document Type: Article
Times cited : (44)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.