Exome Sequencing and Directed Clinical Phenotyping Diagnose Cholesterol Ester Storage Disease Presenting as Autosomal Recessive Hypercholesterolemia
OBJECTIVE - : Autosomal recessive hypercholesterolemia is a rare inherited disorder, characterized by extremely high total and low-density lipoprotein cholesterol levels, that has been previously linked to mutations in LDLRAP1. We identified a family with autosomal recessive hypercholesterolemia not...
Auteurs principaux: | Stitziel, N, Fouchier, S, Sjouke, B, Peloso, G, Moscoso, A, Auer, P, Goel, A, Gigante, B, Barnes, T, Melander, O, Orho-Melander, M, Duga, S, Sivapalaratnam, S, Nikpay, M, Martinelli, N, Girelli, D, Jackson, R, Kooperberg, C, Lange, L, Ardissino, D, McPherson, R, Farrall, M, Watkins, H, Reilly, M, Rader, D |
---|---|
Format: | Journal article |
Langue: | English |
Publié: |
2013
|
Documents similaires
-
Exome sequencing and directed clinical phenotyping diagnose cholesterol ester storage disease presenting as autosomal recessive hypercholesterolemia.
par: Stitziel, N, et autres
Publié: (2013) -
Meta-analysis of gene-level tests for rare variant association
par: Liu, D, et autres
Publié: (2014) -
Meta-analysis of gene-level tests for rare variant association.
par: Liu, D, et autres
Publié: (2014) -
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.
par: Do, R, et autres
Publié: (2014) -
New insights into impaired muscle glycogen synthesis.
par: Leif Groop, et autres
Publié: (2008-01-01)