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CASQ2 variants in Chinese children with catecholaminergic polymorphic ventricular tachycardia
BACKGROUND: Biallelic variants of the CASQ2 are known to cause the autosomal recessive form of catecholaminergic polymorphic ventricular tachycardia (CPVT), an inherited disease that predisposes young individuals to syncope and sudden cardiac death. To date, only about 24 CASQ2 variants have been re...
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| Publicado no: | Mol Genet Genomic Med |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6825949/ https://ncbi.nlm.nih.gov/pubmed/31482657 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.949 |
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