Qin_2018_J.Clin.Lab.Anal_32_e22414

Reference

Title : Rare LPL gene missense mutation in an infant with hypertriglyceridemia - Qin_2018_J.Clin.Lab.Anal_32_e22414
Author(s) : Qin YY , Wei AQ , Shan QW , Xian XY , Wu YY , Liao L , Yan J , Lai ZF , Lin FQ
Ref : J Clin Lab Anal , 32 :e22414 , 2018
Abstract : Qin_2018_J.Clin.Lab.Anal_32_e22414
ESTHER : Qin_2018_J.Clin.Lab.Anal_32_e22414
PubMedSearch : Qin_2018_J.Clin.Lab.Anal_32_e22414
PubMedID: 29479812
Gene_locus related to this paper: human-LPL

Related information

Gene_locus related to this paper: human-LPL

Citations formats

Qin YY, Wei AQ, Shan QW, Xian XY, Wu YY, Liao L, Yan J, Lai ZF, Lin FQ (2018)
Rare LPL gene missense mutation in an infant with hypertriglyceridemia
J Clin Lab Anal 32 :e22414

Qin YY, Wei AQ, Shan QW, Xian XY, Wu YY, Liao L, Yan J, Lai ZF, Lin FQ (2018)
J Clin Lab Anal 32 :e22414