KÖSE, E. Et Al. 2018. Familial chylomicronemia syndrome in two cases due to novel mutation in ApoC- II gene.. Society for the study of Inborn Error of Metabolism 2018 .

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

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

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

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

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