Liu_2020_Front.Genet_11_741

Reference

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

Related information

Gene_locus related to this paper: human-LPL

Citations formats

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