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A novel splice mutation of HERG in a Chinese family with long QT syndrome
Congenital long QT syndrome (LQTS) is a genetically heterogeneous disease in which six ion-channel genes have been identified. The phenotype-genotype relationships of the HERG (human ether-a-go-go-related gene) mutations are not fully understood. The objective of this study is to identify the underl...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Zhejiang University Press
2005
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1389795/ https://ncbi.nlm.nih.gov/pubmed/15973763 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1631/jzus.2005.B0626 |
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