Whole-exome sequencing identifies rare genetic variants in Egyptian patients with hypertrophic cardiomyopathy: a pilot study.

Saved in:
Bibliographic Details
Title: Whole-exome sequencing identifies rare genetic variants in Egyptian patients with hypertrophic cardiomyopathy: a pilot study.
Authors: Negm RE; Biotechnology Department, https://ror.org/03q21mh05Cairo University Faculty of Science, Egypt., Gabre RM; Biotechnology Department, https://ror.org/03q21mh05Cairo University Faculty of Science, Egypt., El-Sherif AA; Chemistry Department, Cairo University Faculty of Science, Egypt., Katta AA; Cardiology Department, National Heart Institute, Egypt., El-Sayed AF; Microbial Genetics Department, Biotechnology Research Institute, National Research Centre, Egypt.; (ECRRM), Egypt Center for Research and Regenerative Medicine, Egypt., ElHefnawi M; Biomedical Informatics and Chemo-Informatics Group, Informatics and Systems Department, National Research Centre, Egypt.
Source: Cardiology in the young [Cardiol Young] 2026 Jul 21, pp. 1-12. Date of Electronic Publication: 2026 Jul 21.
Publication Type: Journal Article
Journal Info: Publisher: Cambridge University Press Country of Publication: England NLM ID: 9200019 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1467-1107 (Electronic) Linking ISSN: 10479511 NLM ISO Abbreviation: Cardiol Young Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1467-1107
DOI:10.1017/S1047951126123622