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Journal Article
Daimagueler, Huelya-Sevcan, Akpulat, Ugur, Oezdemir, Oezkan, Yis, Uluc, Gungor, Serdal, Talim, Beril, Diniz, Gulden, Baydan, Figen, Thiele, Holger, Altmueller, Janine, Nuernberg, Peter and Cirak, Sebahattin (2021). Clinical and genetic characterization of PYROXD1-related myopathy patients from Turkey. Am. J. Med. Genet. A, 185 (6). S. 1678 - 1691. HOBOKEN: WILEY. ISSN 1552-4833
Yis, Uluc, Dixit, Vishal, Isikay, Sedat, Karakaya, Mert, Baydan, Figen, Diniz, Gulden, Polat, Ipek, Hiz-Kurul, Semra and Cirak, Sebahattin (2017). Occipital cortex dysgenesis with white matter changes due to mutations in Laminin alpha 2. Turk. J. Pediatr., 59 (3). S. 338 - 342. ANKARA: TURKISH J PEDIATRICS. ISSN 0041-4301