Publication: Turkish perspective of Jervell and Lange-Nielsen syndrome
dc.contributor.author | Cangül, Hakan | |
dc.contributor.buuauthor | Temel, Şehime Gülsün | |
dc.contributor.buuauthor | Bostan, Özlem Mehtap | |
dc.contributor.buuauthor | Çil, Ergün | |
dc.contributor.department | Tıp Fakültesi | |
dc.contributor.department | Tıbbi Genetik Ana Bilim Dalı | |
dc.contributor.orcid | 0000-0002-9802-0880 | |
dc.contributor.orcid | 0000-0001-7707-2174 | |
dc.contributor.orcid | 0000-0003-3516-0082 | |
dc.contributor.researcherid | AAG-8385-2021 | |
dc.contributor.researcherid | AAG-9324-2021 | |
dc.contributor.researcherid | AAG-8558-2021 | |
dc.contributor.scopusid | 6507885442 | |
dc.contributor.scopusid | 8676936500 | |
dc.contributor.scopusid | 35587943300 | |
dc.date.accessioned | 2023-05-12T11:18:41Z | |
dc.date.available | 2023-05-12T11:18:41Z | |
dc.date.issued | 2013-06 | |
dc.identifier.citation | Temel, Ş. G. vd. (2013). “Turkish perspective of Jervell and Lange-Nielsen syndrome”. Annals of Indian Academy of Neurology, 16(1), 129-130. | |
dc.identifier.endpage | 130 | |
dc.identifier.issn | 0972-2327 | |
dc.identifier.issn | 1998-3549 | |
dc.identifier.issue | 1 | |
dc.identifier.pubmed | 23661983 | |
dc.identifier.scopus | 2-s2.0-84875695272 | |
dc.identifier.startpage | 129 | |
dc.identifier.uri | https://doi.org/10.4103/0972-2327.107703 | |
dc.identifier.uri | https://journals.lww.com/annalsofian/Fulltext/2013/16010/Turkish_perspective_of_Jervell_and_Lange_Nielsen.29.aspx | |
dc.identifier.uri | http://hdl.handle.net/11452/32646 | |
dc.identifier.volume | 16 | |
dc.identifier.wos | 000316907100029 | |
dc.indexed.wos | SCIE | |
dc.language.iso | en | |
dc.publisher | Wolters Kluwer Medknow Publications | |
dc.relation.collaboration | Yurt dışı | |
dc.relation.collaboration | Yurt içi | |
dc.relation.journal | Annals of Indian Academy of Neurology | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.subject | Neurosciences & neurology | |
dc.subject | Deafness | |
dc.subject | Children | |
dc.subject.emtree | Echocardiography | |
dc.subject.emtree | Exercise test | |
dc.subject.emtree | Faintness | |
dc.subject.emtree | Family history | |
dc.subject.emtree | Hearing impairment | |
dc.subject.emtree | Heart depolarization | |
dc.subject.emtree | Holter monitoring | |
dc.subject.emtree | Human | |
dc.subject.emtree | Letter | |
dc.subject.emtree | Long QT syndrome | |
dc.subject.emtree | Turkey (republic) | |
dc.subject.scopus | Potassium Channels; Jervell-Lange Nielsen Syndrome; Torsade Des Pointes | |
dc.subject.wos | Clinical neurology | |
dc.title | Turkish perspective of Jervell and Lange-Nielsen syndrome | |
dc.type | Letter | |
dc.wos.quartile | Q4 | |
dc.wos.quartile | Q2 | |
dspace.entity.type | Publication | |
local.contributor.department | Tıp Fakültesi/Tıbbi Genetik Ana Bilim Dalı | |
local.indexed.at | Scopus | |
local.indexed.at | WOS |