Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families. (February 2018) - Kocoglu, Cemile; Gundogdu, Asli; Kocaman, Gulsen; Kahraman-Koytak, Pinar; Uluc, Kayihan; Kiziltan, Gunes; Caglayan, Ahmet Okay; Bilguvar, Kaya; Vural, Atay; Basak, A. Nazli