Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families

Kocoglu, CemileGundogdu, AsliKocaman, GulsenKAHRAMAN KOYTAK, PINARULUÇ, KAYIHANKiziltan, GunesCaglayan, Ahmet OkayBilguv, KayaVural, AtayBasak, A. Nazli2020-10-222020-10-222018-02-01Kocoglu C., Gundogdu A., Kocaman G., KAHRAMAN KOYTAK P., ULUÇ K., Kiziltan G., Caglayan A. O. , Bilguv K., Vural A., Basak A. N. , -Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families-, NEUROLOGY-GENETICS, cilt.4, 2018http://hdl.handle.net/20.500.12645/24571Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 familiesArticleWOS:0004305017000108504871697110.1212/nxg.000000000000021829379883