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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Detalles Bibliográficos
Autores principales: Li, Qirui, Guo, Ruolan, Gao, Lu, Cui, Lang, Zhao, Zhihui, Yu, Xia, Yuan, Yue, Xu, Xiwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6825949/
https://www.ncbi.nlm.nih.gov/pubmed/31482657
http://dx.doi.org/10.1002/mgg3.949

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6825949/
https://www.ncbi.nlm.nih.gov/pubmed/31482657
http://dx.doi.org/10.1002/mgg3.949

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