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Author/Creator Coskun, Turgay

4. Clinical phenotype, biochemical profile, and treatment in 19 patients with arginase 1 deficiency. Issue 3 (1st April 2016)

Authors:
Huemer, Martina; Carvalho, Daniel R.; Brum, Jaime M.; Ünal, Özlem; Coskun, Turgay; Weisfeld‐Adams, James D.; Schrager, Nina L.; Scholl‐Bürgi, Sabine; Schlune, Andrea; Donner, Markus G.; Hersberger, Martin; Gemperle, Claudio; Riesner, Brunhilde; Ulmer, Hanno; Häberle, Johannes; Karall, Daniela
Journal:
Journal of inherited metabolic disease
Issue:
Volume 39:Issue 3(2016)
Page Start:
331
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

5. Expanding the clinical spectrum of mitochondrial 3‐hydroxy‐3‐methylglutaryl‐CoA synthase deficiency with Turkish cases harboring novel HMGCS2 gene mutations and literature review. Issue 7 (7th April 2020)

Authors:
Kılıç, Mustafa; Dorum, Sevil; Topak, Ali; Yazıcı, Mutlu U.; Ezgu, Fatih S.; Coskun, Turgay
Journal:
American journal of medical genetics
Issue:
Volume 182:Issue 7(2020)
Page Start:
1608
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗