KÖSE, E. Et Al. 2018. Familial chylomicronemiasyndrome in two cases due to novel mutation in ApoC- II gene.. Society for the study of Inborn Error of Metabolism 2018 , (Athens, Greece).

KÖSE, E., ARMAGAN, C., TEKE KISA, P., & ARSLAN, N., (2018). Familial chylomicronemiasyndrome in two cases due to novel mutation in ApoC- II gene. . Society for the study of Inborn Error of Metabolism 2018, Athens, Greece

KÖSE, ENGİN Et Al. "Familial chylomicronemiasyndrome in two cases due to novel mutation in ApoC- II gene.," Society for the study of Inborn Error of Metabolism 2018, Athens, Greece, 2018

KÖSE, ENGİN Et Al. "Familial chylomicronemiasyndrome in two cases due to novel mutation in ApoC- II gene.." Society for the study of Inborn Error of Metabolism 2018 , Athens, Greece, 2018

KÖSE, E. Et Al. (2018) . "Familial chylomicronemiasyndrome in two cases due to novel mutation in ApoC- II gene.." Society for the study of Inborn Error of Metabolism 2018 , Athens, Greece.

@conferencepaper{conferencepaper, author={ENGİN KÖSE Et Al. }, title={Familial chylomicronemiasyndrome in two cases due to novel mutation in ApoC- II gene.}, congress name={Society for the study of Inborn Error of Metabolism 2018}, city={Athens}, country={Greece}, year={2018}}