Microcephaly, Epilepsy, and Diabetes Syndrome 1: A Moroccan Case Report of Novel Compound Heterozygous IER3IP1 Mutations and Literature Review
By: H Jelti, K Khabbache, S Bouressas, F Hacht, A Oulmaati and A Lamzouri
DOI: https://doi.org/10.2478/bjmg-2025-0006 | Journal eISSN: 2199-5761 (formerly 1311-0160) | Journal ISSN: 1311-0160
Language: English
Published on: Oct 8, 2025
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
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© 2025 H Jelti, K Khabbache, S Bouressas, F Hacht, A Oulmaati, A Lamzouri, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.