Title : Novel pathogenic variant combination in LPL causing familial chylomicronemia syndrome in an Asian family and experimental validation in vitro: a case report - Shi_2022_Transl.Pediatr_11_1717 |
Author(s) : Shi H , Wang Z |
Ref : Transl Pediatr , 11 :1717 , 2022 |
Abstract : Shi_2022_Transl.Pediatr_11_1717 |
ESTHER : Shi_2022_Transl.Pediatr_11_1717 |
PubMedSearch : Shi_2022_Transl.Pediatr_11_1717 |
PubMedID: 36345447 |
Gene_locus related to this paper: human-LPL |
Gene_locus related to this paper: human-LPL |
Shi H, Wang Z (2022)
Novel pathogenic variant combination in LPL causing familial chylomicronemia syndrome in an Asian family and experimental validation in vitro: a case report
Transl Pediatr
11 :1717
Shi H, Wang Z (2022)
Transl Pediatr
11 :1717