AKTUĞLU ZEYBEK, A. Ç. Et Al. 2015. Citrin deficiency: An infant incidentally detected by phenylketonuria screening with a novel mutation in SLC25A 13 gene. Genetic Counseling , vol.26, no.4 , 409-413.

AKTUĞLU ZEYBEK, A. Ç., KIYKIM, E., ZÜBARİOĞLU, T., CANSEVER, M. Ş., CEYLANER, S., & Erkan, T., (2015). Citrin deficiency: An infant incidentally detected by phenylketonuria screening with a novel mutation in SLC25A 13 gene. Genetic Counseling , vol.26, no.4, 409-413.

AKTUĞLU ZEYBEK, AYŞE Et Al. "Citrin deficiency: An infant incidentally detected by phenylketonuria screening with a novel mutation in SLC25A 13 gene," Genetic Counseling , vol.26, no.4, 409-413, 2015

AKTUĞLU ZEYBEK, AYŞE Ç. Et Al. "Citrin deficiency: An infant incidentally detected by phenylketonuria screening with a novel mutation in SLC25A 13 gene." Genetic Counseling , vol.26, no.4, pp.409-413, 2015

AKTUĞLU ZEYBEK, A. Ç. Et Al. (2015) . "Citrin deficiency: An infant incidentally detected by phenylketonuria screening with a novel mutation in SLC25A 13 gene." Genetic Counseling , vol.26, no.4, pp.409-413.

@article{article, author={AYŞE ÇİĞDEM AKTUĞLU ZEYBEK Et Al. }, title={Citrin deficiency: An infant incidentally detected by phenylketonuria screening with a novel mutation in SLC25A 13 gene}, journal={Genetic Counseling}, year=2015, pages={409-413} }