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Microcephaly, Epilepsy, and Diabetes Syndrome 1: A Moroccan Case Report of Novel Compound Heterozygous IER3IP1 Mutations and Literature Review

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Bibliographic Details
Published in:Balkan Journal of Medical Genetics
Format: Online Article RSS Article
Published: 2025
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container_title Balkan Journal of Medical Genetics
description
discipline_display Life Sciences & Biology
discipline_facet Life Sciences & Biology
format Online Article
RSS Article
genre Journal Article
id rss_article:28692
institution FRELIP
journal_source_facet Balkan Journal of Medical Genetics
publishDate 2025
publishDateSort 2025
record_format rss_article
spellingShingle Microcephaly, Epilepsy, and Diabetes Syndrome 1: A Moroccan Case Report of Novel Compound Heterozygous IER3IP1 Mutations and Literature Review
— — — — — — Genetics
Biological Sciences
Life Sciences & Biology
sub_discipline_display Biological Sciences
sub_discipline_facet Biological Sciences
subject_display — — — — — — Genetics
Biological Sciences
Life Sciences & Biology
— — — — — — Genetics
Biological Sciences
Life Sciences & Biology
subject_facet — — — — — — Genetics
Biological Sciences
Life Sciences & Biology
title Microcephaly, Epilepsy, and Diabetes Syndrome 1: A Moroccan Case Report of Novel Compound Heterozygous IER3IP1 Mutations and Literature Review
title_auth Microcephaly, Epilepsy, and Diabetes Syndrome 1: A Moroccan Case Report of Novel Compound Heterozygous IER3IP1 Mutations and Literature Review
title_full Microcephaly, Epilepsy, and Diabetes Syndrome 1: A Moroccan Case Report of Novel Compound Heterozygous IER3IP1 Mutations and Literature Review
title_fullStr Microcephaly, Epilepsy, and Diabetes Syndrome 1: A Moroccan Case Report of Novel Compound Heterozygous IER3IP1 Mutations and Literature Review
title_full_unstemmed Microcephaly, Epilepsy, and Diabetes Syndrome 1: A Moroccan Case Report of Novel Compound Heterozygous IER3IP1 Mutations and Literature Review
title_short Microcephaly, Epilepsy, and Diabetes Syndrome 1: A Moroccan Case Report of Novel Compound Heterozygous IER3IP1 Mutations and Literature Review
title_sort microcephaly, epilepsy, and diabetes syndrome 1: a moroccan case report of novel compound heterozygous ier3ip1 mutations and literature review
topic — — — — — — Genetics
Biological Sciences
Life Sciences & Biology
url https://sciendo.com/article/10.2478/bjmg-2025-0006