A Frequent Mutation in the FTL Gene Causing Hyperferritinemia Cataract Syndrome in Turkish Population Is c.-160A>G

por Balta, Burhan, Erdoğan, Murat, Kiraz, Aslıhan, Korkmaz, Serdal, Ağadayı, Alperen
Publicado 2019

A c.1244G>A (p.Arg415Gln) mutation in SH3BP2 gene causes cherubism in a Turkish family: Report of a family with review of the literature

por Sekerci, Ahmet E., Balta, Burhan, Hu, Ying, Reichenberger, Ernst J., Etoz, Osman A., Nazlim, Sinan, Bayrakdar, Ibrahim S.
Publicado 2014

The Genetic Analysis of Cystic Fibrosis Patients with Seven Novel Mutations in the CFTR Gene in the Central Anatolian Region of Turkey

por Erdoğan, Murat, Köse, Mehmet, Pekcan, Sevgi, Hangül, Melih, Balta, Burhan, Kiraz, Aslıhan, Akıncı Gönen, Gizem, Gül Zamani, Ayşe, Selman Yıldırım, Mahmut, Ramaslı Gürsoy, Tuğba, Ezgu, Fatih, Şişmanlar Eyüpoğlu, Tuğba, Tana Aslan, Ayse
Publicado 2021