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Ghada M.H. Abdel-Salam, Ashleigh E. Schaffer, Maha S. Zaki, Tracy Dixon-Salazar, Inas S. Mostafa, Hanan H. Afifi and Joseph G. Gleeson A homozygous IER3IP1 mutation causes microcephaly with simplified gyral pattern, epilepsy, and permanent neonatal diabetes syndrome (MEDS) American Journal of Medical Genetics Part A 158A

Version of Record online: 18 SEP 2012 | DOI: 10.1002/ajmg.a.35583

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