Blockade of TRPV2 is a Novel Therapy for Cardiomyopathy in Muscular Dystrophy

Muscular dystrophy and dilated cardiomyopathy are intractable diseases and their treatment options are very limited. Transient receptor potential cation channel subfamily V, member 2 (TRPV2), is a stretch-sensitive Ca<sup>2+</sup>-permeable channel that causes sustained intracellular Ca&...

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Bibliographic Details
Main Authors: Yuko Iwata, Tsuyoshi Matsumura
Format: Article
Language:English
Published: MDPI AG 2019-08-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/20/16/3844