Mutation Analysis of the Iduronate-2-Sulfatase Gene among Egyptian Patients with Hunter Syndrome
to 5% of RPL cases are caused by genetic factors, which can include gene mutations or chromosomal abnormalities.An increasing number of research have concentrated on genetic variables, namely single nucleotide polymorphism (SNP) (Abdi-Shayan et al., 2016).
Authors
- Mona L. Essawi (ORCID: https://orcid.org/0000-0002-1067-8873)
- Heba Hassan (ORCID: https://orcid.org/0000-0002-9567-0896)
- M. Khalil (ORCID: https://orcid.org/0000-0002-1750-9335)
- Ekram Fateen (ORCID: https://orcid.org/0000-0002-0777-0417)
- Nouran Mohamed Sedky
- Mona Aglan (ORCID: https://orcid.org/0000-0002-0908-0639)
- Mona Mohamed Ibrahim (ORCID: https://orcid.org/0000-0003-3407-4983)
- Nurhadi Ibrahim (ORCID: https://orcid.org/0000-0003-3682-0820)
Publication Details
- Journal
- Middle East Journal of Medical Genetics
- Published
- 2025-09-24
- DOI
- https://doi.org/10.21608/mxe.2025.362459.1036
- Primary Topic
- Lysosomal Storage Disorders Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Research Centre