Prenatal diagnosis of glucose-6-phosphatase catalytic subunit 3 deficiency (Dursun syndrome) using whole-exome sequencing: A case report of severe fetal cardiomyopathy in a consanguineous family
- DOI
- 10.1177/03000605261476146
- Published
- 2026-08
- Container
- Journal of International Medical Research
- Publisher
- SAGE Publications
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1177/03000605261476146,
title = {Prenatal diagnosis of glucose-6-phosphatase catalytic subunit 3 deficiency (Dursun syndrome) using whole-exome sequencing: A case report of severe fetal cardiomyopathy in a consanguineous family},
author = {Sarah M Ghazali and Rima S Bader},
year = {2026},
journal = {Journal of International Medical Research},
doi = {10.1177/03000605261476146},
url = {https://doi.org/10.1177/03000605261476146}
}RIS
TY - JOUR TI - Prenatal diagnosis of glucose-6-phosphatase catalytic subunit 3 deficiency (Dursun syndrome) using whole-exome sequencing: A case report of severe fetal cardiomyopathy in a consanguineous family AU - Sarah M Ghazali AU - Rima S Bader PY - 2026 JO - Journal of International Medical Research DO - 10.1177/03000605261476146 UR - https://doi.org/10.1177/03000605261476146 ER -
APA
Ghazali, S. M., & Bader, R. S. (2026). Prenatal diagnosis of glucose-6-phosphatase catalytic subunit 3 deficiency (Dursun syndrome) using whole-exome sequencing: A case report of severe fetal cardiomyopathy in a consanguineous family. Journal of International Medical Research. https://doi.org/10.1177/03000605261476146
Source records
- crossref · retrieved 2026-09-26T01:46:00.708Z