Molecular defect in familial lecithin:cholesterol acyltransferase (LCAT) deficiency: a single nucleotide insertion in LCAT gene causes a complete deficient type of the disease (Q28235384)
Jump to navigation
Jump to search
scientific article (publication date: 31 December 1991)
Language | Label | Description | Also known as |
---|---|---|---|
English | Molecular defect in familial lecithin:cholesterol acyltransferase (LCAT) deficiency: a single nucleotide insertion in LCAT gene causes a complete deficient type of the disease |
scientific article (publication date: 31 December 1991) |
Statements
Molecular defect in familial lecithin:cholesterol acyltransferase (LCAT) deficiency: a single nucleotide insertion in LCAT gene causes a complete deficient type of the disease (English)
0 references
31 December 1991
0 references
181
0 references
3
0 references
933-40
0 references