المؤلفون: Oselusi, Samson O., Dube, Phumuzile, Odugbemi, Adeshina I., Akinyede, Kolajo A., Ilori, Tosin L., Egieyeh, Elizabeth, Sibuyi, Nicole RS., Meyer, Mervin, Madiehe, Abram M., Wyckoff, Gerald J., Egieyeh, Samuel A.

المساهمون: National Research Foundation

المصدر: Computers in Biology and Medicine ; volume 169, page 107927 ; ISSN 0010-4825

الاتاحة: http://dx.doi.org/10.1016/j.compbiomed.2024.107927
https://api.elsevier.com/content/article/PII:S0010482524000118?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0010482524000118?httpAccept=text/plain

المؤلفون: Crotti, L, Insolia, R, Pedrazzini, M, Ferrandi, C, Tosin, L, Moncalvo, C, Turco, A, Agnetti, A, De Ferrari, G, Schwartz, P, Crotti Lia, Insolia R, Pedrazzini M, Ferrandi C, Tosin L, Moncalvo C, Turco A, Agnetti A, De Ferrari Gm, Schwartz Pj.

مصطلحات الفهرس: KCNQ1, cardiac potassium channel, long qt syndrome, mutation, MED/11 - MALATTIE DELL'APPARATO CARDIOVASCOLARE, info:eu-repo/semantics/article

URL: http://hdl.handle.net/10281/190150
https://link.springer.com/article/10.1007/s00439-006-0247-5#Sec29
info:eu-repo/semantics/altIdentifier/pmid/17438609
volume:120
issue:6
firstpage:912
lastpage:912
numberofpages:1
journal:HUMAN GENETICS

المؤلفون: Crotti L, Insolia R, Pedrazzini M, Ferrandi C, Tosin L, Moncalvo C, Turco A, Agnetti A, De Ferrari G, Schwartz PJ.

المساهمون: Crotti L, Insolia R, Pedrazzini M, Ferrandi C, Tosin L, Moncalvo C, Turco A, Agnetti A, De Ferrari G, Schwartz PJ.

Relation: firstpage:912; lastpage:912; numberofpages:1; journal:HUMAN GENETICS; http://hdl.handle.net/2318/1737204

الاتاحة: http://hdl.handle.net/2318/1737204

المؤلفون: CROTTI, LIA, Insolia R, Pedrazzini M, Ferrandi C, Tosin L, Moncalvo C, Turco A, Agnetti A, DE FERRARI, GAETANO, Schwartz P.j.

المساهمون: Crotti, Lia, Insolia, R, Pedrazzini, M, Ferrandi, C, Tosin, L, Moncalvo, C, Turco, A, Agnetti, A, DE FERRARI, Gaetano, Schwartz, P. j.

مصطلحات موضوعية: KCNQ1

وصف الملف: STAMPA

Relation: volume:120; firstpage:912; lastpage:912; journal:HUMAN GENETICS; http://hdl.handle.net/11571/35326

الاتاحة: http://hdl.handle.net/11571/35326

المؤلفون: CROTTI, LIA, SCHWARTZ, PETER, Ferrandi C, Insolia R, Pedrazzini M, Tosin L, Veia A, Turco A, De Ferrari Gm

المساهمون: Crotti, Lia, Ferrandi, C, Insolia, R, Pedrazzini, M, Tosin, L, Veia, A, Turco, A, De Ferrari, Gm, Schwartz, Peter

مصطلحات موضوعية: SCN5A

وصف الملف: STAMPA

Relation: volume:120; firstpage:911; lastpage:912; journal:HUMAN GENETICS; http://hdl.handle.net/11571/35329

الاتاحة: http://hdl.handle.net/11571/35329

المؤلفون: Crotti, Lia, Ferrandi, C, Insolia, R, Pedrazzini, M, Tosin, L, Veia, A, Turco, A, De Ferrari, GM, Schwartz, PJ

المساهمون: Crotti, L, Ferrandi, C, Insolia, R, Pedrazzini, M, Tosin, L, Veia, A, Turco, A, De Ferrari, G, Schwartz, P

مصطلحات موضوعية: SCN5A. cardiac sodium channel, long qt syndrome, mutation, MED/11 - MALATTIE DELL'APPARATO CARDIOVASCOLARE

وصف الملف: STAMPA

Relation: info:eu-repo/semantics/altIdentifier/pmid/17438607; volume:120; issue:6; firstpage:911; lastpage:912; numberofpages:2; journal:HUMAN GENETICS; http://hdl.handle.net/10281/190143; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-34247847875; https://link.springer.com/article/10.1007/s00439-006-0247-5

الاتاحة: http://hdl.handle.net/10281/190143
https://link.springer.com/article/10.1007/s00439-006-0247-5

المؤلفون: Crotti Lia, Insolia R, Pedrazzini M, Ferrandi C, Tosin L, Moncalvo C, Turco A, Agnetti A, De Ferrari Gm, Schwartz Pj.

المساهمون: Crotti, L, Insolia, R, Pedrazzini, M, Ferrandi, C, Tosin, L, Moncalvo, C, Turco, A, Agnetti, A, De Ferrari, G, Schwartz, P

مصطلحات موضوعية: KCNQ1, cardiac potassium channel, long qt syndrome, mutation, MED/11 - MALATTIE DELL'APPARATO CARDIOVASCOLARE

وصف الملف: STAMPA

Relation: info:eu-repo/semantics/altIdentifier/pmid/17438609; volume:120; issue:6; firstpage:912; lastpage:912; numberofpages:1; journal:HUMAN GENETICS; http://hdl.handle.net/10281/190150; https://link.springer.com/article/10.1007/s00439-006-0247-5#Sec29

الاتاحة: http://hdl.handle.net/10281/190150
https://link.springer.com/article/10.1007/s00439-006-0247-5#Sec29

المؤلفون: lia crotti, Insolia R, Pedrazzini M, Ferrandi C, Tosin L, Moncalvo C, Turco A, Agnetti A, Gm, Ferrari, Pj, Schwartz

المصدر: Europe PubMed Central

مصطلحات موضوعية: Long QT Syndrome, Amino Acid Substitution, Case-Control Studies, KCNQ1 Potassium Channel, Mutation, Missense, Humans, Female, Child

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::b03b89b9f9670d416ff21ff749b9026b
https://pubmed.ncbi.nlm.nih.gov/17438609

المؤلفون: Crotti, L, Ferrandi, C, Insolia, R, Pedrazzini, M, Tosin, L, Veia, A, Turco, A, De Ferrari, G, Schwartz, P, Crotti, Lia, De Ferrari, GM, Schwartz, PJ

مصطلحات الفهرس: SCN5A. cardiac sodium channel, long qt syndrome, mutation, MED/11 - MALATTIE DELL'APPARATO CARDIOVASCOLARE, info:eu-repo/semantics/article

URL: http://hdl.handle.net/10281/190143
https://link.springer.com/article/10.1007/s00439-006-0247-5
info:eu-repo/semantics/altIdentifier/pmid/17438607
volume:120
issue:6
firstpage:911
lastpage:912
numberofpages:2
journal:HUMAN GENETICS

المؤلفون: lia crotti, Ferrandi, C., Insolia, R., Pedrazzini, M., Tosin, L., Veia, A., Turco, A., Ferrari, G. M., Schwartz, P. J.

المصدر: Scopus-Elsevier
ResearcherID
Europe PubMed Central

مصطلحات موضوعية: Long QT Syndrome, Adolescent, Amino Acid Substitution, Torsades de Pointes, Mutation, Missense, Humans, Muscle Proteins, Female, Sodium Channels, NAV1.5 Voltage-Gated Sodium Channel

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::73e37c10c55d706138ee8716ca5177e0
http://www.scopus.com/inward/record.url?eid=2-s2.0-34247847875&partnerID=MN8TOARS