Related Experiment Video
Updated: May 13, 2026
03:45
Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
A silent composite hemoglobinopathy characterized by gene sequencing
A Zorai1, I Moumni, I Benmansour
1Laboratory of Molecular and Cellular Hematology, Pasteur Institute of Tunis, University of Tunis.
Archives De L'Institut Pasteur De Tunis
|March 7, 2013
Summary
This study details a Tunisian woman
Area of Science:
- Hematology
- Genetics
- Molecular Biology
Background:
- Chronic anemia requires thorough investigation.
- Genetic factors can cause persistent anemia.
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01:31Translation
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