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Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families.
Kocoglu C, Gundogdu A, Kocaman G, Kahraman-Koytak P, Uluc K, Kiziltan G, Caglayan AO, Bilguvar K, Vural A, Basak AN. Kocoglu C, et al. Among authors: kocaman g. Neurol Genet. 2018 Jan 18;4(1):e218. doi: 10.1212/NXG.0000000000000218. eCollection 2018 Feb. Neurol Genet. 2018. PMID: 29379883 Free PMC article. No abstract available.
Two-point discrimination in diabetic patients.
Eryilmaz M, Koçer A, Kocaman G, Dikici S. Eryilmaz M, et al. Among authors: kocaman g. J Diabetes. 2013 Dec;5(4):442-8. doi: 10.1111/1753-0407.12055. Epub 2013 Jun 4. J Diabetes. 2013. PMID: 23560652
66 results