Sener, L. Et Al. 2019. Identification of red blood cell membrane defects in a patient with hereditary spherocytosis using next-generation sequencing technology and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. MOLECULAR MEDICINE REPORTS , vol.19, no.5 , 3912-3922.

Sener, L., Aktan, M., Albeniz, G., Sener, A., Üstek, D., & Albeniz, I., (2019). Identification of red blood cell membrane defects in a patient with hereditary spherocytosis using next-generation sequencing technology and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. MOLECULAR MEDICINE REPORTS , vol.19, no.5, 3912-3922.

Sener, Leyla Et Al. "Identification of red blood cell membrane defects in a patient with hereditary spherocytosis using next-generation sequencing technology and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry," MOLECULAR MEDICINE REPORTS , vol.19, no.5, 3912-3922, 2019

Sener, Leyla T. Et Al. "Identification of red blood cell membrane defects in a patient with hereditary spherocytosis using next-generation sequencing technology and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry." MOLECULAR MEDICINE REPORTS , vol.19, no.5, pp.3912-3922, 2019

Sener, L. Et Al. (2019) . "Identification of red blood cell membrane defects in a patient with hereditary spherocytosis using next-generation sequencing technology and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry." MOLECULAR MEDICINE REPORTS , vol.19, no.5, pp.3912-3922.

@article{article, author={Leyla TÜRKER ŞENER Et Al. }, title={Identification of red blood cell membrane defects in a patient with hereditary spherocytosis using next-generation sequencing technology and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry}, journal={MOLECULAR MEDICINE REPORTS}, year=2019, pages={3912-3922} }