Evaluation of Patients Diagnosed with Congenital Glycosylation Defects: A Rainbow of Inherited Metabolic Disorders.

MLA

Kılavuz, Sebile, et al. “Evaluation of Patients Diagnosed with Congenital Glycosylation Defects: A Rainbow of Inherited Metabolic Disorders.” Journal of the Child / Çocuk Dergisi, vol. 23, no. 3, Sept. 2023, pp. 31–40. EBSCOhost, https://doi.org/10.26650/jchild.2023.1345981.

APA

Kılavuz, S., Bulut, D., Kor, D., Yılmaz, B. Ş., Bişgin, A., Demir, F., Atmış, B., Alabaz, D., Mungan, N., & Yılmaz, M. (2023). Evaluation of Patients Diagnosed with Congenital Glycosylation Defects: A Rainbow of Inherited Metabolic Disorders. Journal of the Child / Çocuk Dergisi, 23(3), 31–40. https://doi.org/10.26650/jchild.2023.1345981

Chicago

Kılavuz, Sebile, Derya Bulut, Deniz Kor, Berna Şeker Yılmaz, Atil Bişgin, Fadli Demir, Bahriye Atmış, Derya Alabaz, Neslihan Mungan, and Mustafa Yılmaz. 2023. “Evaluation of Patients Diagnosed with Congenital Glycosylation Defects: A Rainbow of Inherited Metabolic Disorders.” Journal of the Child / Çocuk Dergisi 23 (3): 31–40. doi:10.26650/jchild.2023.1345981.