Consequences of SUR2[A478V] Mutation in Skeletal Muscle of Murine Model of Cantu Syndrome
(1) Background: Cantu syndrome (CS) arises from gain-of-function (GOF) mutations in the <i>ABCC9</i> and <i>KCNJ8</i> genes, which encode ATP-sensitive K<sup>+</sup> (KATP) channel subunits SUR2 and Kir6.1, respectively. Most CS patients have mutations in SUR2, th...
Main Authors: | , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
MDPI AG
2021-07-01
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Series: | Cells |
Subjects: | |
Online Access: | https://www.mdpi.com/2073-4409/10/7/1791 |