DIAPH1 homozygous mutation associated with microcephaly, blindness, and seizures


ACER H. , CANPOLAT M. , KAYA ÖZÇORA G. D. , KUMANDAŞ S.

EPNS 2017 - 12th European Paediatric Neurology Society CongressLyon, France 20- 24 June 2017, 20 - 24 June 2017, cilt.21, ss.60