Genetic evaluation of cardiomyopathies in Qatar identifies enrichment of pathogenic sarcomere gene variants and possible founder disease mutations in the Arabs

Genetic evaluation of cardiomyopathies in Qatar identifies enrichment of pathogenic sarcomere gene variants and possible founder disease mutations in the Arabs

<h3>Background</h3><p dir="ltr">Hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM) are serious inherited heart diseases with various causative mutations identified. The full spectrum of causative mutations remains to be discovered, especially in understudi...

Full description

Saved in:
Bibliographic Details
Main Author: Kholoud N. Al‐Shafai (18459009) (author)
Other Authors: Mohammed Al‐Hashemi (18459012) (author), Chidambaram Manickam (18434100) (author), Rania Musa (18459015) (author), Senthil Selvaraj (314873) (author), Najeeb Syed (12561967) (author), Fazulur Vempalli (18459018) (author), Muneera Ali (18459021) (author), Magdi Yacoub (6893000) (author), Xavier Estivill (23803) (author)
Published: 2021
Subjects:
Biological sciences
Genetics
Biomedical and clinical sciences
Cardiovascular medicine and haematology
cardiomyopathy
targeted sequencing
genetic variants
Qatar
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items