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A novel GJA1 mutation causing familial oculodentodigital dysplasia with dilated cardiomyopathy and arrhythmia

Detalles Bibliográficos
Autores principales: Wittlieb-Weber, Carol A., Haude, Katrina M., Fong, Chin-To, Vinocur, Jeffrey M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5412637/
https://www.ncbi.nlm.nih.gov/pubmed/28491627
http://dx.doi.org/10.1016/j.hrcr.2015.08.013
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author Wittlieb-Weber, Carol A.
Haude, Katrina M.
Fong, Chin-To
Vinocur, Jeffrey M.
author_facet Wittlieb-Weber, Carol A.
Haude, Katrina M.
Fong, Chin-To
Vinocur, Jeffrey M.
author_sort Wittlieb-Weber, Carol A.
collection PubMed
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spelling pubmed-54126372017-05-10 A novel GJA1 mutation causing familial oculodentodigital dysplasia with dilated cardiomyopathy and arrhythmia Wittlieb-Weber, Carol A. Haude, Katrina M. Fong, Chin-To Vinocur, Jeffrey M. HeartRhythm Case Rep Case Report Elsevier 2015-10-13 /pmc/articles/PMC5412637/ /pubmed/28491627 http://dx.doi.org/10.1016/j.hrcr.2015.08.013 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
Wittlieb-Weber, Carol A.
Haude, Katrina M.
Fong, Chin-To
Vinocur, Jeffrey M.
A novel GJA1 mutation causing familial oculodentodigital dysplasia with dilated cardiomyopathy and arrhythmia
title A novel GJA1 mutation causing familial oculodentodigital dysplasia with dilated cardiomyopathy and arrhythmia
title_full A novel GJA1 mutation causing familial oculodentodigital dysplasia with dilated cardiomyopathy and arrhythmia
title_fullStr A novel GJA1 mutation causing familial oculodentodigital dysplasia with dilated cardiomyopathy and arrhythmia
title_full_unstemmed A novel GJA1 mutation causing familial oculodentodigital dysplasia with dilated cardiomyopathy and arrhythmia
title_short A novel GJA1 mutation causing familial oculodentodigital dysplasia with dilated cardiomyopathy and arrhythmia
title_sort novel gja1 mutation causing familial oculodentodigital dysplasia with dilated cardiomyopathy and arrhythmia
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5412637/
https://www.ncbi.nlm.nih.gov/pubmed/28491627
http://dx.doi.org/10.1016/j.hrcr.2015.08.013
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