Novel dilated cardiomyopathy associated to Calreticulin and Myo7A gene mutation in Usher syndrome

Novel dilated cardiomyopathy associated to Calreticulin and Myo7A gene mutation in Usher syndrome

Abstract We report a novel cardiomyopathy associated to Usher syndrome and related to combined mutation of MYO7A and Calreticulin genes. A 37‐year‐old man with deafness and vision impairment because of retinitis pigmentosa since childhood and a MYO7A gene mutation suggesting Usher syndrome, develope...

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Bibliographic Details
Main Authors: Andrea Frustaci, Alessandro De Luca, Nicola Galea, Romina Verardo, Valentina Guida, Rosalba Carrozzo, Cristina Chimenti, Emanuela Frustaci, Luigi Sansone, Matteo Antonio Russo
Format: Article
Language:English
Published: Wiley 2021-06-01
Series:ESC Heart Failure
Subjects:
Usher syndrome
MYO7A
CALR
Calreticulin
Cardiomyocyte disconnection
Online Access:https://doi.org/10.1002/ehf2.13260

Internet

https://doi.org/10.1002/ehf2.13260

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