Human RyR2 (Ryanodine Receptor 2) Loss-of-Function Mutations: Clinical Phenotypes and In Vitro Characterization.

(Circulation. Arrhythmia and electrophysiology, v14.9:e010013)

Abstract

[Figure: see text].

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TitleHuman RyR2 (Ryanodine Receptor 2) Loss-of-Function Mutations: Clinical Phenotypes and In Vitro Characterization.
Date2021-09-01
Issue nameCirculation. Arrhythmia and electrophysiology
Issue numberv14.9:e010013
DOI10.1161/CIRCEP.121.010013
PubMed34546788
AuthorsLi Y, Wei J, Guo W, Sun B, Estillore JP, Wang R, Yoruk A, Roston TM, Sanatani S, Wilde AAM, Gollob MH, Roberts JD, Tseng ZH, Jensen HK & Chen SRW
Keywordscaffeine, death, mutation, phenotype, ryanodine
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