Bozkurt, T. Et Al. 2021. Re-analysis of whole-exome sequencing data reveals a novel splicing variant in the SLC2A1 in a patient with GLUT1 Deficiency Syndrome 1 accompanied by hemangioma: a case report. BMC MEDICAL GENOMICS , vol.14, no.1 .

Bozkurt, T., ALANAY, Y., ISIK, U., & SEZERMAN, O. U., (2021). Re-analysis of whole-exome sequencing data reveals a novel splicing variant in the SLC2A1 in a patient with GLUT1 Deficiency Syndrome 1 accompanied by hemangioma: a case report. BMC MEDICAL GENOMICS , vol.14, no.1.

Bozkurt, Tugce Et Al. "Re-analysis of whole-exome sequencing data reveals a novel splicing variant in the SLC2A1 in a patient with GLUT1 Deficiency Syndrome 1 accompanied by hemangioma: a case report," BMC MEDICAL GENOMICS , vol.14, no.1, 2021

Bozkurt, Tugce Et Al. "Re-analysis of whole-exome sequencing data reveals a novel splicing variant in the SLC2A1 in a patient with GLUT1 Deficiency Syndrome 1 accompanied by hemangioma: a case report." BMC MEDICAL GENOMICS , vol.14, no.1, 2021

Bozkurt, T. Et Al. (2021) . "Re-analysis of whole-exome sequencing data reveals a novel splicing variant in the SLC2A1 in a patient with GLUT1 Deficiency Syndrome 1 accompanied by hemangioma: a case report." BMC MEDICAL GENOMICS , vol.14, no.1.

@article{article, author={Tugce Bozkurt Et Al. }, title={Re-analysis of whole-exome sequencing data reveals a novel splicing variant in the SLC2A1 in a patient with GLUT1 Deficiency Syndrome 1 accompanied by hemangioma: a case report}, journal={BMC MEDICAL GENOMICS}, year=2021}