PCSK9 Variants in Familial Hypercholesterolemia: A Comprehensive Synopsis
Author:
Publisher
Frontiers Media SA
Subject
Genetics(clinical),Genetics,Molecular Medicine
Reference139 articles.
1. A PCSK9 variant and familial combined hyperlipidaemia.;Abifadel;J. Med. Genet.,2008
2. Identification and characterization of new gain-of-function mutations in the PCSK9 gene responsible for autosomal dominant hypercholesterolemia.;Abifadel;Atherosclerosis,2012
3. Mutations and polymorphisms in the proprotein convertase subtilisin kexin 9 (PCSK9) gene in cholesterol metabolism and disease.;Abifadel;Hum. Mutat.,2009
4. Mutations in PCSK9 cause autosomal dominant hypercholesterolemia.;Abifadel;Nat. Genet.,2003
5. The genetic spectrum of familial hypercholesterolemia in Pakistan.;Ahmed;Clin. Chim. Acta.,2013
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