Related Experiment Video
Updated: Apr 15, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
A case of Morfan syndrome
Bryan Hiscox, Jenny Hu, Lorraine C Young1
1Department of Medicine, University of California at Los Angeles (UCLA) David Geffen School of Medicine, 200 UCLA Medical Plaza, Ste 450, Los Angeles, CA 90095, USA. lcyoung@mednet.ucla.edu.
No abstract available in PubMed .
More Related Videos
09:37Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information
Published on: August 15, 2019
08:22A Robust Polymerase Chain Reaction-based Assay for Quantifying Cytosine-guanine-guanine Trinucleotide Repeats in Fragile X Mental Retardation-1 Gene
Published on: September 16, 2019
Related Concept Videos
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Aneurysm I: Introduction
Cystic Fibrosis: Management
Sinus disease and chronic...
Mitral Stenosis II: Clinical features and Diagnostic Tests
Mitral Stenosis I: Introduction