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A homozygous IER3IP1 mutation causes microcephaly with simplified gyral pattern, epilepsy, and permanent neonatal diabetes syndrome (MEDS)

✍ Scribed by Prof. Ghada M.H. Abdel-Salam; Ashleigh E. Schaffer; Maha S. Zaki; Tracy Dixon-Salazar; Inas S. Mostafa; Hanan H. Afifi; Joseph G. Gleeson


Book ID
115549410
Publisher
John Wiley and Sons
Year
2012
Tongue
English
Weight
350 KB
Volume
158A
Category
Article
ISSN
1552-4825

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