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Genetic Counseling (Geneva, Switzerland)|August 5, 2009
A Turkish newborn infant with cerebellar agenesis/neonatal diabetes mellitus and PTF1A mutationE Tutak, M Satar, H Yapicioğlu, et al.
European Journal of Neurology|November 23, 2006
Fatigue and sleep disturbance in multiple sclerosisH Kaynak, A Altintaş, D Kaynak, et al.
Journal of the Neurological Sciences|May 30, 2006
The R110C mutation in Notch3 causes variable clinical features in two Turkish families with CADASIL syndromeZ O Uyguner, A Siva, H Kayserili, et al.
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