[HTML][HTML] Novel missense variants in LCAT and APOB genes in an Italian kindred with familial lecithin: cholesterol acyltransferase deficiency and …

P Conca, S Pileggi, S Simonelli, E Boer… - Journal of Clinical …, 2012 - Elsevier
BACKGROUND: Lecithin: cholesterol acyltransferase (LCAT) is responsible for cholesterol
esterification in plasma. Mutations of LCAT gene cause familial LCAT deficiency, a …

Novel missense variants in LCAT and APOB genes in an Italian kindred with familial lecithin: cholesterol acyltransferase deficiency and hypobetalipoproteinemia

P Conca, S Pileggi, S Simonelli… - Journal of clinical …, 2012 - pubmed.ncbi.nlm.nih.gov
Background Lecithin: cholesterol acyltransferase (LCAT) is responsible for cholesterol
esterification in plasma. Mutations of LCAT gene cause familial LCAT deficiency, a …

Novel missense variants in LCAT and APOB genes in an Italian kindred with familial lecithin: cholesterol acyltransferase deficiency and hypobetalipoproteinemia.

P Conca, S Pileggi, S Simonelli, E Boer… - Journal of Clinical …, 2012 - europepmc.org
Background Lecithin: cholesterol acyltransferase (LCAT) is responsible for cholesterol
esterification in plasma. Mutations of LCAT gene cause familial LCAT deficiency, a …

[PDF][PDF] Novel missense variants in LCAT and APOB genes in an Italian kindred with familial lecithin: cholesterol acyltransferase deficiency and …

P Conca, S Pileggi, S Simonelli, E Boer… - Journal of Clinical …, 2012 - researchgate.net
BACKGROUND: Lecithin: cholesterol acyltransferase (LCAT) is responsible for cholesterol
esterification in plasma. Mutations of LCAT gene cause familial LCAT deficiency, a …

Novel missense variants in LCAT and APOB genes in an Italian kindred with familial lecithin: cholesterol acyltransferase deficiency and hypobetalipoproteinemia.

P Conca, S Pileggi, S Simonelli, E Boer… - JOURNAL OF …, 2012 - iris.unimore.it
BACKGROUND: Lecithin: cholesterol acyltransferase (LCAT) is responsible for cholesterol
esterification in plasma. Mutations of LCAT gene cause familial LCAT deficiency, a …

Novel missense variants in LCAT and APOB genes in an Italian kindred with familial lecithin: cholesterol acyltransferase deficiency and hypobetalipoproteinemia

P Conca, S Pileggi, S Simonelli, E Boer… - Journal of Clinical …, 2012 - infona.pl
Lecithin: cholesterol acyltransferase (LCAT) is responsible for cholesterol esterification in
plasma. Mutations of LCAT gene cause familial LCAT deficiency, a metabolic disorder …

[HTML][HTML] Novel missense variants in LCAT and APOB genes in an Italian kindred with familial lecithin: cholesterol acyltransferase deficiency and …

P Conca, S Pileggi, S Simonelli, E Boer… - Journal of Clinical …, 2012 - ncbi.nlm.nih.gov
Background Lecithin: cholesterol acyltransferase (LCAT) is responsible for cholesterol
esterification in plasma. Mutations of LCAT gene cause familial LCAT deficiency, a …

[HTML][HTML] Novel missense variants in LCAT and APOB genes in an Italian kindred with familial lecithin: cholesterol acyltransferase deficiency and …

P Conca, S Pileggi, S Simonelli, E Boer… - Journal of Clinical …, 2012 - lipidjournal.com
Background Lecithin: cholesterol acyltransferase (LCAT) is responsible for cholesterol
esterification in plasma. Mutations of LCAT gene cause familial LCAT deficiency, a …

[PDF][PDF] Novel missense variants in LCAT and APOB genes in an Italian kindred with familial lecithin: cholesterol acyltransferase deficiency and …

P Conca, S Pileggi, S Simonelli, E Boer… - Journal of Clinical …, 2012 - cyberleninka.org
BACKGROUND: Lecithin: cholesterol acyltransferase (LCAT) is responsible for cholesterol
esterification in plasma. Mutations of LCAT gene cause familial LCAT deficiency, a …

[PDF][PDF] Novel missense variants in LCAT and APOB genes in an Italian kindred with familial lecithin: cholesterol acyltransferase deficiency and …

P Conca, S Pileggi, S Simonelli, E Boer… - Journal of Clinical …, 2012 - academia.edu
BACKGROUND: Lecithin: cholesterol acyltransferase (LCAT) is responsible for cholesterol
esterification in plasma. Mutations of LCAT gene cause familial LCAT deficiency, a …