Genetic and phenotypic heterogeneity in familial lecithin: cholesterol acyltransferase (LCAT) deficiency. Six newly identified defective alleles further contribute to the structural heterogeneity in this disease (Q33891534)
Jump to navigation
Jump to search
scientific article
Language | Label | Description | Also known as |
---|---|---|---|
English | Genetic and phenotypic heterogeneity in familial lecithin: cholesterol acyltransferase (LCAT) deficiency. Six newly identified defective alleles further contribute to the structural heterogeneity in this disease |
scientific article |
Statements
1 reference
Genetic and phenotypic heterogeneity in familial lecithin: cholesterol acyltransferase (LCAT) deficiency. Six newly identified defective alleles further contribute to the structural heterogeneity in this disease (English)
1 reference
H Funke
1 reference
A von Eckardstein
1 reference
P H Pritchard
1 reference
A E Hornby
1 reference
H Wiebusch
1 reference
C Motti
1 reference
M R Hayden
1 reference
C Dachet
1 reference
B Jacotot
1 reference
U Gerdes
1 reference
1 February 1993
1 reference
1 reference
677-683
1 reference
1 reference
1 reference
1 reference
1 reference
Identifiers
1 reference
1 reference
1 reference