Whole-exome sequencing identifies rare genetic variants in Egyptian patients with hypertrophic cardiomyopathy: a pilot study.
- DOI
- 10.1017/s1047951126123622
- Published
- 2026 Jul 21
- Container
- Cardiology in the young
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1017/s1047951126123622,
title = {Whole-exome sequencing identifies rare genetic variants in Egyptian patients with hypertrophic cardiomyopathy: a pilot study.},
author = {Negm RE and Gabre RM and El-Sherif AA and Katta AA and El-Sayed AF and ElHefnawi M},
year = {2026},
journal = {Cardiology in the young},
doi = {10.1017/s1047951126123622},
url = {https://doi.org/10.1017/s1047951126123622}
}RIS
TY - JOUR TI - Whole-exome sequencing identifies rare genetic variants in Egyptian patients with hypertrophic cardiomyopathy: a pilot study. AU - Negm RE AU - Gabre RM AU - El-Sherif AA AU - Katta AA AU - El-Sayed AF AU - ElHefnawi M PY - 2026 JO - Cardiology in the young DO - 10.1017/s1047951126123622 UR - https://doi.org/10.1017/s1047951126123622 ER -
APA
RE, N., RM, G., AA, E., AA, K., AF, E., & M, E. (2026). Whole-exome sequencing identifies rare genetic variants in Egyptian patients with hypertrophic cardiomyopathy: a pilot study.. Cardiology in the young. https://doi.org/10.1017/s1047951126123622
Source records
- pubmed · retrieved 2026-09-26T02:24:59.004Z