| Title : Deficiency of lecithin:cholesterol acyltransferase due to compound heterozygosity of two novel mutations (Gly33Arg and 30 bp ins) in the LCAT gene - |
| Author(s) : Wiebusch H , Cullen P , Owen JS , Collins D , Sharp PS , Funke H , Assmann G |
| Ref : Hum Mol Genet , 4 :143 , 1995 |
| PubMedID: 7711728 |
| Gene_locus related to this paper: human-LCAT |
| Gene_locus related to this paper: human-LCAT |
Wiebusch H, Cullen P, Owen JS, Collins D, Sharp PS, Funke H, Assmann G (1995)
Deficiency of lecithin:cholesterol acyltransferase due to compound heterozygosity of two novel mutations (Gly33Arg and 30 bp ins) in the LCAT gene
Hum Mol Genet
4 :143
Wiebusch H, Cullen P, Owen JS, Collins D, Sharp PS, Funke H, Assmann G (1995)
Hum Mol Genet
4 :143