A homozygous IER3IP1 mutation causes microcephaly with simplified gyral pattern, epilepsy, and permanent neonatal diabetes syndrome (MEDS).
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| Description | scientific article published on 18 September 2012 |
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author: Ghada M Abdel-Salam Inas S Mostafa Hanan H. Afifi Joseph G Gleeson Ashleigh Schaffer Maha Zaki |
| Publication date | September 18, 2012 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |