Association between the catechol-o-methyltransferase val158met polymorphism with susceptibility and severity of carpal tunnel syndrome
E Erkol İnal, P Eroğlu, O Görükmez, Ş Özemri Sağ, T Yakut
A novel mutation in a newborn baby leading to glycogen storage disease type Ia
S Dorum, O Gorukmez
An investigation of the COMT gene Val158Met polymorphism in patients admitted to the emergency department because of synthetic cannabinoid use
Y Nennicioglu, H Kaya, S Eraybar, S Atmaca, O Gorukmez, E Armagan
Achondrogenesis type 2 in a newborn with a novel mutation on the COL2A1 gene
P Dogan, IG Varal, O Gorukmez, MO Akkurt, A Akdag