Browsing by Author "Ugur, Iseri"
Biallelic loss of EEF1D function links heat shock response pathway to autosomal recessive intellectual disability. Ugur, Iseri; Yucesan, Emrah; Tuncer, FN; Calik, M; Kesim, Y; Altiokka, Uzun; Ozbek, U (2019-05-01)
SYNE1 related cerebellar ataxia presents with variable phenotypes in a consanguineous family from Turkey. Yucesan, Emrah; Ugur, Iseri; Bilgic, B; Gormez, Z; Bakir, Gungor; Sarac, A; Ozdemir, O; Sagiroglu, M; Gurvit, H; Hanagasi, H; Ozbek, U (2017-12-01)