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