Shi_2022_Transl.Pediatr_11_1717

Reference

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

Related information

Gene_locus related to this paper: human-LPL

Citations formats

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