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KCNH2 mutation c.3099_3112del causes congenital long QT syndrome type 2 with gender differences

Crossref DOI link: https://doi.org/10.1016/j.clinsp.2023.100285

Published Print: 2023-01

Update policy: https://doi.org/10.1016/elsevier_cm_policy

Authors

Ke, ZunPing

Li, Chao

Bai, Gang

Tan, Li

Wang, JunFeng

Zhou, Ming

Zhou, JianHua

Chen, Shi-You http://orcid.org/0000-0002-0297-8649
Dong, Xiao http://orcid.org/0000-0002-4687-8324
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Text and Data Mining valid from 2023-01-01

Text and Data Mining valid from 2023-01-01

Version of Record valid from 2023-09-07
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This article is maintained by: Elsevier

Article Title: KCNH2 mutation c.3099_3112del causes congenital long QT syndrome type 2 with gender differences

Journal Title: Clinics

CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.clinsp.2023.100285

Content Type: article

Copyright: © 2023 HCFMUSP. Published by Elsevier España, S.L.U.