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Updated: Jun 19, 2025

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Whole-Exome Sequencing Detecting a Recurrent Pathogenic Mutation, HFE p.His63Asp (H63D) in COVID-19 Patients and Its

Rashid Mir1, Imadeldin Elfaki2, Mohammad A Alanazi1

  • 1Department of Medical Lab Technology, Prince Fahad Bin Sultan Chair for Biomedical Research, Faculty of Applied Medical Sciences, University of Tabuk, 71491 Tabuk, Saudi Arabia.

Discovery Medicine
|July 26, 2024
PubMed
Abstract

Keywords:
GWASscoronavirus – COVID-19 – whole exome sequencing -

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