Kim_2024_BMC.Endocr.Disord_24_47

Reference

Title : Familial chylomicronemia syndrome: case reports of siblings with deletions of the GPIHBP1 gene - Kim_2024_BMC.Endocr.Disord_24_47
Author(s) : Kim KY , Heo YJ , Ko JM , Lee YA , Shin CH , Ki CS , Lee YJ
Ref : BMC Endocr Disord , 24 :47 , 2024
Abstract : Kim_2024_BMC.Endocr.Disord_24_47
ESTHER : Kim_2024_BMC.Endocr.Disord_24_47
PubMedSearch : Kim_2024_BMC.Endocr.Disord_24_47
PubMedID: 38622573

Related information

Citations formats

Kim KY, Heo YJ, Ko JM, Lee YA, Shin CH, Ki CS, Lee YJ (2024)
Familial chylomicronemia syndrome: case reports of siblings with deletions of the GPIHBP1 gene
BMC Endocr Disord 24 :47

Kim KY, Heo YJ, Ko JM, Lee YA, Shin CH, Ki CS, Lee YJ (2024)
BMC Endocr Disord 24 :47