KCNQ1 G219E and TRPM4 T160M polymorphisms are involved in the pathogenesis of long QT syndrome: A case report

RATIONALE: Long QT syndrome (LQTS) is an inheritable disease characterized by prolonged QT interval on the electrocardiogram. The pathogenesis of LQTS is related to mutations in LQTS-susceptible genes encoding cardiac ion channel proteins or subunits. PATIENT CONCERNS: Here, we reported a 37-year-ol...

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Detalles Bibliográficos
Autores principales: Zhao, Yang, Feng, Min, Shang, Lu-Xiang, Sun, Hua-xin, Zhou, Xian-Hui, Lu, Yan-Mei, Zhang, Ling, Xing, Qiang, Li, Yao-dong, Tang, Bao-Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
3400
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7808457/
https://www.ncbi.nlm.nih.gov/pubmed/33466149
http://dx.doi.org/10.1097/MD.0000000000024032

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7808457/
https://www.ncbi.nlm.nih.gov/pubmed/33466149
http://dx.doi.org/10.1097/MD.0000000000024032

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