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Familial long QT syndrome and late development of dilated cardiomyopathy in a child with a KCNQ1 mutation: A case report

Detalles Bibliográficos
Autores principales: Allen, Kiona Y., Vetter, Victoria L., Shah, Maully J., O’Connor, Matthew J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5412615/
https://www.ncbi.nlm.nih.gov/pubmed/28491650
http://dx.doi.org/10.1016/j.hrcr.2015.10.011
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author Allen, Kiona Y.
Vetter, Victoria L.
Shah, Maully J.
O’Connor, Matthew J.
author_facet Allen, Kiona Y.
Vetter, Victoria L.
Shah, Maully J.
O’Connor, Matthew J.
author_sort Allen, Kiona Y.
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spelling pubmed-54126152017-05-10 Familial long QT syndrome and late development of dilated cardiomyopathy in a child with a KCNQ1 mutation: A case report Allen, Kiona Y. Vetter, Victoria L. Shah, Maully J. O’Connor, Matthew J. HeartRhythm Case Rep Case Report Elsevier 2015-12-18 /pmc/articles/PMC5412615/ /pubmed/28491650 http://dx.doi.org/10.1016/j.hrcr.2015.10.011 Text en © 2016 Heart Rhythm Society. Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Allen, Kiona Y.
Vetter, Victoria L.
Shah, Maully J.
O’Connor, Matthew J.
Familial long QT syndrome and late development of dilated cardiomyopathy in a child with a KCNQ1 mutation: A case report
title Familial long QT syndrome and late development of dilated cardiomyopathy in a child with a KCNQ1 mutation: A case report
title_full Familial long QT syndrome and late development of dilated cardiomyopathy in a child with a KCNQ1 mutation: A case report
title_fullStr Familial long QT syndrome and late development of dilated cardiomyopathy in a child with a KCNQ1 mutation: A case report
title_full_unstemmed Familial long QT syndrome and late development of dilated cardiomyopathy in a child with a KCNQ1 mutation: A case report
title_short Familial long QT syndrome and late development of dilated cardiomyopathy in a child with a KCNQ1 mutation: A case report
title_sort familial long qt syndrome and late development of dilated cardiomyopathy in a child with a kcnq1 mutation: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5412615/
https://www.ncbi.nlm.nih.gov/pubmed/28491650
http://dx.doi.org/10.1016/j.hrcr.2015.10.011
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