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Clinical features of 27 Turkish Propionic acidemia patients with 12 novel mutations.
Kör D, Şeker-Yılmaz B, Bulut FD, Kılavuz S, Öktem M, Ceylaner S, Yıldızdaş D, Önenli-Mungan N. Kör D, et al. Among authors: ceylaner s. Turk J Pediatr. 2019;61(3):330-336. doi: 10.24953/turkjped.2019.03.003. Turk J Pediatr. 2019. PMID: 31916709 Free article.
Kor D, Seker-Yilmaz B, Bulut FD, Kilavuz S, Oktem M, Ceylaner S, Yildizdas D, Onenli-Mungan N. Clinical features of 27 Turkish Propionic acidemia patients with 12 novel mutations. ...
Kor D, Seker-Yilmaz B, Bulut FD, Kilavuz S, Oktem M, Ceylaner S, Yildizdas D, Onenli-Mungan N. Clinical features of 27 …
Two novel missense mutations in nonketotic hyperglycinemia.
Yilmaz BS, Kor D, Ceylaner S, Mert GG, Incecik F, Kartal E, Mungan NO. Yilmaz BS, et al. Among authors: ceylaner s. J Child Neurol. 2015 May;30(6):789-92. doi: 10.1177/0883073814535499. Epub 2014 May 16. J Child Neurol. 2015. PMID: 24838951
p.Val452Ile mutation of the SLC25A13 gene in a Turkish patient with citrin deficiency.
Şeker-Yılmaz B, Kör D, Tümgör G, Ceylaner S, Önenli-Mungan N. Şeker-Yılmaz B, et al. Among authors: ceylaner s. Turk J Pediatr. 2017;59(3):311-314. doi: 10.24953/turkjped.2017.03.012. Turk J Pediatr. 2017. PMID: 29376577 Free article.
Seker-Yilmaz B, Kor D, Tumgor G, Ceylaner S, Onenli-Mungan N. p.Val452Ile mutation of the SLC25A13 gene in a Turkish patient with citrin deficiency. ...
Seker-Yilmaz B, Kor D, Tumgor G, Ceylaner S, Onenli-Mungan N. p.Val452Ile mutation of the SLC25A13 gene in a Turkish patient w …
249 results