المؤلفون: Duchatelet S., CROTTI, LIA, Peat R.A., Denjoy I., Itoh H, Berthet M., Ohno S., Fressart V., MONTI, MARIA CRISTINA, CROCAMO, CRISTINA, PEDRAZZINI, MATTEO, DAGRADI, FEDERICA, Vicentini A., Klug D., Brink P.A., Goosen A., Swan H., Toivonen L., Lahtinen A.M., Kontula K., Shimizu W., Horie M., George AL J.r., Trégouët D.A., Guicheney P., SCHWARTZ, PETER

المساهمون: Duchatelet, S., Crotti, Lia, Peat, R. A., Denjoy, I., Itoh, H, Berthet, M., Ohno, S., Fressart, V., Monti, MARIA CRISTINA, Crocamo, Cristina, Pedrazzini, Matteo, Dagradi, Federica, Vicentini, A., Klug, D., Brink, P. A., Goosen, A., Swan, H., Toivonen, L., Lahtinen, A. M., Kontula, K., Shimizu, W., Horie, M., George AL, J. r., Trégouët, D. A., Guicheney, P., Schwartz, Peter

مصطلحات موضوعية: Association studies, Genetics, Ion channel, Long-QT syndrome, Polymorphism, Risk factor

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/23856471; info:eu-repo/semantics/altIdentifier/wos/WOS:000323542700007; volume:6; issue:4; firstpage:354; lastpage:361; numberofpages:8; journal:CIRCULATION, CARDIOVASCULAR GENETICS; http://hdl.handle.net/11571/896246Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84884514304

الإتاحة: https://doi.org/10.1161/CIRCGENETICS.113.000023Test
http://hdl.handle.net/11571/896246Test

المؤلفون: Federica Dagradi, Alfred L. George, Rachel Peat, Lauri Toivonen, Lia Crotti, Sabine Duchatelet, Seiko Ohno, Cristina Crocamo, Peter J. Schwartz, Alessandro Vicentini, Heikki Swan, Matteo Pedrazzini, Didier Klug, David-Alexandre Trégouët, Pascale Guicheney, Isabelle Denjoy, Annukka M. Lahtinen, Kimmo Kontula, Myriam Berthet, Maria Cristina Monti, Hideki Itoh, Minoru Horie, Althea Goosen, Paul A. Brink, Wataru Shimizu, Véronique Fressart

المساهمون: Duchatelet, S, Crotti, L, Peat, R, Denjoy, I, Itoh, H, Berthet, M, Ohno, S, Fressart, V, Monti, M, Crocamo, C, Pedrazzini, M, Dagradi, F, Vicentini, A, Klug, D, Brink, P, Goosen, A, Swan, H, Toivonen, L, Lahtinen, A, Kontula, K, Shimizu, W, Horie, M, George, A, Trégouët, D, Guicheney, P, Schwartz, P

المصدر: Circ. Cardiovasc. Genet. 6, 354-361 (2013)

مصطلحات موضوعية: Male, ERG1 Potassium Channel, 030204 cardiovascular system & hematology, Pharmacology, Long-QT syndrome, Sudden cardiac death, Cohort Studies, 0302 clinical medicine, Gene Frequency, Risk Factors, Databases, Genetic, Genetics (clinical), Allele, 0303 health sciences, education.field_of_study, Association Studies, Genetics, Ion Channel, Long-qt Syndrome, Polymorphism, Risk Factor, 3. Good health, Long QT Syndrome, KCNQ1 Potassium Channel, Female, medicine.symptom, Ion channel, Case-Control Studie, Cardiology and Cardiovascular Medicine, Human, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Heterozygote, Genotype, Long QT syndrome, Population, BIO/18 - GENETICA, Biology, Asymptomatic, QT interval, Sudden death, Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, Genetic, Internal medicine, medicine, Humans, cardiovascular diseases, education, Alleles, MED/01 - STATISTICA MEDICA, 030304 developmental biology, Genetic association, Case-control study, Ether-A-Go-Go Potassium Channel, MED/11 - MALATTIE DELL'APPARATO CARDIOVASCOLARE, medicine.disease, Ether-A-Go-Go Potassium Channels, Association studie, Case-Control Studies, Cohort Studie

وصف الملف: STAMPA; application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4510a0d295be720b9900c06c3de7a567Test
http://hdl.handle.net/10281/138287Test