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Updated: Apr 28, 2026

03:45
Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
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Mitochondrial tRNA mutations manifest not only as hypertrophic cardiomyopathy but also as noncompaction--reply
Carla Giordano1, Camillo Autore2, Giulia d'Amati3
1Department of Radiological, Oncological and Pathological Sciences, Sapienza University of Rome.
Human Pathology
|June 19, 2014
Abstract
No abstract available in PubMed .
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