Gunes, D. Et Al. 2023. A very rare cause of hypertrygliseridemia in infancy: A novel mutation in glycerol-3-phosphate dehydrogenase 1 (GPD1) gene. Journal of Pediatric Endocrinology and Metabolism , vol.36, no.7 , 704-707.

Gunes, D., Kalaycik Sengul, O., & Senturk, L., (2023). A very rare cause of hypertrygliseridemia in infancy: A novel mutation in glycerol-3-phosphate dehydrogenase 1 (GPD1) gene. Journal of Pediatric Endocrinology and Metabolism , vol.36, no.7, 704-707.

Gunes, Dilek, Ozlem Kalaycik Sengul, And Leyli Senturk. "A very rare cause of hypertrygliseridemia in infancy: A novel mutation in glycerol-3-phosphate dehydrogenase 1 (GPD1) gene," Journal of Pediatric Endocrinology and Metabolism , vol.36, no.7, 704-707, 2023

Gunes, Dilek Et Al. "A very rare cause of hypertrygliseridemia in infancy: A novel mutation in glycerol-3-phosphate dehydrogenase 1 (GPD1) gene." Journal of Pediatric Endocrinology and Metabolism , vol.36, no.7, pp.704-707, 2023

Gunes, D. Kalaycik Sengul, O. And Senturk, L. (2023) . "A very rare cause of hypertrygliseridemia in infancy: A novel mutation in glycerol-3-phosphate dehydrogenase 1 (GPD1) gene." Journal of Pediatric Endocrinology and Metabolism , vol.36, no.7, pp.704-707.

@article{article, author={Dilek GÜNEŞ Et Al. }, title={A very rare cause of hypertrygliseridemia in infancy: A novel mutation in glycerol-3-phosphate dehydrogenase 1 (GPD1) gene}, journal={Journal of Pediatric Endocrinology and Metabolism}, year=2023, pages={704-707} }