Approaching the facts between genetic mutation and clinical practice of hypertrophic cardiomyopathy: A case report with RAF1 770C>T mutant

INTRODUCTION: Hypertrophic cardiomyopathy (HCM) is one of the most common cardiomyopathies, which induces sudden cardiac death. Several mutants have been identified among HCM cases. METHODS AND RESULTS: A 10-month female infant who experienced cough, fever, aggressive exertional dyspnea, and recurre...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Xiaoqin, Zhou, Kaiyu, Hua, Yimin, Li, Yifei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
3400
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5402577/
https://www.ncbi.nlm.nih.gov/pubmed/27631234
http://dx.doi.org/10.1097/MD.0000000000004815

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5402577/
https://www.ncbi.nlm.nih.gov/pubmed/27631234
http://dx.doi.org/10.1097/MD.0000000000004815

Ejemplares similares