DIAPH1 homozygous mutation associated with microcephaly, blindness, and seizures
Authors:
- H. AcerHAH. Acer
- M. CanpolatMCM. Canpolat
- G.K. ÖzçoraGÖG.K. Özçora
- S. KumandaşSKS. Kumandaş
- 1 June 2017
- journal article
- Published by Elsevier in European Journal of Paediatric Neurology
- Vol. 21, e60