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Discovery of Digenic Mutation, KCNH2 c.1898A >C and JUP c.916dupA, in a Chinese Family with Long QT Syndrome via Whole-Exome Sequencing
Long QT syndrome (LQTS), which is caused by an ion channel–related gene mutation, is a malignant heart disease with a clinical course of a high incidence of ventricular fibrillation and sudden cardiac death in the young. Mutations in KCNH2 (which encodes potassium voltage-gated channel subfamily H m...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Compuscript
2020-07-01
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| Colecção: | Cardiovascular Innovations and Applications |
| Assuntos: | |
| Acesso em linha: | https://www.ingentaconnect.com/content/cscript/cvia/2020/00000004/00000004/art00004 |
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