| Title : Familial chylomicronemia syndrome caused by compound heterozygous mutation of lipoprotein lipase gene: a case report and review of literature - Huang_2022_Clin.Chim.Acta__ |
| Author(s) : Huang Y , Qin Y , Liao L , Lin F |
| Ref : Clinica Chimica Acta , : , 2022 |
| Abstract : Huang_2022_Clin.Chim.Acta__ |
| ESTHER : Huang_2022_Clin.Chim.Acta__ |
| PubMedSearch : Huang_2022_Clin.Chim.Acta__ |
| PubMedID: 36252692 |
| Gene_locus related to this paper: human-LPL |
| Gene_locus related to this paper: human-LPL |
Huang Y, Qin Y, Liao L, Lin F (2022)
Familial chylomicronemia syndrome caused by compound heterozygous mutation of lipoprotein lipase gene: a case report and review of literature
Clinica Chimica Acta
:
Huang Y, Qin Y, Liao L, Lin F (2022)
Clinica Chimica Acta
: