Familial chylomicronemia syndrome in two cases due to novel mutation in ApoC- II gene.

KÖSE E., ARMAĞAN C., TEKE KISA P., ARSLAN N.

Society for the study of Inborn Error of Metabolism 2018, 4 - 07 September 2018

  • Publication Type: Conference Paper / Summary Text
  • Dokuz Eylül University Affiliated: Yes