Title : Analysis of a Chinese Pedigree With Familial Chylomicronemia Syndrome Reveals Two Novel LPL Mutations by Whole-Exome Sequencing - Liu_2020_Front.Genet_11_741 |
Author(s) : Liu Y , Lan Z , Zhao F , Zhang S , Zhang W |
Ref : Front Genet , 11 :741 , 2020 |
Abstract : Liu_2020_Front.Genet_11_741 |
ESTHER : Liu_2020_Front.Genet_11_741 |
PubMedSearch : Liu_2020_Front.Genet_11_741 |
PubMedID: 32765589 |
Gene_locus related to this paper: human-LPL |
Gene_locus related to this paper: human-LPL |
Liu Y, Lan Z, Zhao F, Zhang S, Zhang W (2020)
Analysis of a Chinese Pedigree With Familial Chylomicronemia Syndrome Reveals Two Novel LPL Mutations by Whole-Exome Sequencing
Front Genet
11 :741
Liu Y, Lan Z, Zhao F, Zhang S, Zhang W (2020)
Front Genet
11 :741