Ucar, H. K. Et Al. 2023. A NOVEL VARIATION OF GAMT IN CEREBRAL CREATINE DEFICIENCY SYNDROME, FIRST COMPLETE HOMOZYGOUS DELETION OF GAMT. Genetika Belgrade , vol.55, no.1 , 415-426.

Ucar, H. K., Bulut, F. D., Gurbuz, B. B., Dilek, O., & Guney, I., (2023). A NOVEL VARIATION OF GAMT IN CEREBRAL CREATINE DEFICIENCY SYNDROME, FIRST COMPLETE HOMOZYGOUS DELETION OF GAMT. Genetika Belgrade , vol.55, no.1, 415-426.

Ucar, Habibe Et Al. "A NOVEL VARIATION OF GAMT IN CEREBRAL CREATINE DEFICIENCY SYNDROME, FIRST COMPLETE HOMOZYGOUS DELETION OF GAMT," Genetika Belgrade , vol.55, no.1, 415-426, 2023

Ucar, Habibe K. Et Al. "A NOVEL VARIATION OF GAMT IN CEREBRAL CREATINE DEFICIENCY SYNDROME, FIRST COMPLETE HOMOZYGOUS DELETION OF GAMT." Genetika Belgrade , vol.55, no.1, pp.415-426, 2023

Ucar, H. K. Et Al. (2023) . "A NOVEL VARIATION OF GAMT IN CEREBRAL CREATINE DEFICIENCY SYNDROME, FIRST COMPLETE HOMOZYGOUS DELETION OF GAMT." Genetika Belgrade , vol.55, no.1, pp.415-426.

@article{article, author={Habibe Koc Ucar Et Al. }, title={A NOVEL VARIATION OF GAMT IN CEREBRAL CREATINE DEFICIENCY SYNDROME, FIRST COMPLETE HOMOZYGOUS DELETION OF GAMT}, journal={Genetika Belgrade}, year=2023, pages={415-426} }