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pro vyhledávání: '"Hugo Ariel Garro"'
Autor:
Hyun Sok Yoo, Nancy Medina, María Alejandra von Wulffen, Natalia Ciampi, Analia Paolucci, Hugo Ariel Garro, Mario Bruno Principato, Rafael Salvador Acunzo, Justo Carbajales
Publikováno v:
International Journal of Arrhythmia, Vol 22, Iss 1, Pp 1-6 (2021)
Abstract Background The congenital long QT syndrome type 2 is caused by mutations in KCNH2 gene that encodes the alpha subunit of potassium channel Kv11.1. The carriers of the pathogenic variant of KCNH2 gene manifest a phenotype characterized by pro
Externí odkaz:
https://doaj.org/article/13ba0334fed04b749e6b025b1ec2493b