Title : Case Report: Next-Generation Sequencing Identified a Novel Pair of Compound-Heterozygous Mutations of LPL Gene Causing Lipoprotein Lipase Deficiency - Li_2022_Front.Genet_13_831133 |
Author(s) : Li Y , Hu M , Han L , Feng L , Yang L , Chen X , Du T , Yao H |
Ref : Front Genet , 13 :831133 , 2022 |
Abstract : Li_2022_Front.Genet_13_831133 |
ESTHER : Li_2022_Front.Genet_13_831133 |
PubMedSearch : Li_2022_Front.Genet_13_831133 |
PubMedID: 35309119 |
Gene_locus related to this paper: human-LPL |
Gene_locus related to this paper: human-LPL |
Li Y, Hu M, Han L, Feng L, Yang L, Chen X, Du T, Yao H (2022)
Case Report: Next-Generation Sequencing Identified a Novel Pair of Compound-Heterozygous Mutations of LPL Gene Causing Lipoprotein Lipase Deficiency
Front Genet
13 :831133
Li Y, Hu M, Han L, Feng L, Yang L, Chen X, Du T, Yao H (2022)
Front Genet
13 :831133