January 11, 2023Open Access

Calmodulin Mutations in Human Disease

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Abstract

release channel, ryanodine receptor 2 (RyR2). Here, we review the research that has been done to identify calmodulinopathic CaM mutations and evaluate the mechanisms underlying their role in disease.

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Hussey et al. (Wed,) studied this question.

synapsesocial.com/papers/6a07b47944ff8ad339f69b22 https://doi.org/https://doi.org/10.1080/19336950.2023.2165278

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1Human Calmodulin Mutations2018 · 123 citations
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3Cardiac Hypertrophy: The Good, the Bad, and the Ugly2003 · 1,458 citations
4Ca 2+ -sensitive inactivation of L-type Ca 2+ channels depends on multiple cytoplasmic amino acid sequences of the α 1C subunit1998 · 189 citations
5Ryanodine receptor–bound calmodulin is essential to protect against catecholaminergic polymorphic ventricular tachycardia2019 · 29 citations

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