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:
Case Report
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

Internet

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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