Evaluation of electrocardiographic parameters in patients with hearing loss genotyped for the connexin 26 gene (GJB2) mutations()

INTRODUCTION: Several studies have associated congenital sensorineural hearing loss in children with prolongation of the cardiac parameter QTc. The cause of this association is unknown. At the same time, mutations in GJB2, which encodes connexin 26, are the most common cause of congenital hearing im...

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Detalles Bibliográficos
Autores principales: Sanecka, Agnieszka, Biernacka, Elzbieta Katarzyna, Sosna, Magdalena, Mueller-Malesinska, Malgorzata, Ploski, Rafal, Skarzynski, Henryk, Piotrowicz, Ryszard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9442716/
https://www.ncbi.nlm.nih.gov/pubmed/27177978
http://dx.doi.org/10.1016/j.bjorl.2016.02.008

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9442716/
https://www.ncbi.nlm.nih.gov/pubmed/27177978
http://dx.doi.org/10.1016/j.bjorl.2016.02.008

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