Mutation in the PCSK9 Gene in Omani Arab Subjects with Autosomal Dominant Hypercholesterolemia and its Effect on PCSK9 Protein Structure

Proprotein convertase subtilisin/kexin type (PCSK9) is a crucial protein in LDL cholesterol (LDL-C) metabolism by virtue of its pivotal role in the degradation of the LDL receptor. Mutations in the PCSK9 gene have previously been found to segregate with autosomal dominant familial hypercholesterolem...

Descrición completa

Gardado en:
Detalles Bibliográficos
Main Authors: Al-Waili, Khalid, Al-Zidi, Ward Al-Muna, Al-Abri, Abdul Rahim, Al-Rasadi, Khalid, Al-Sabti, Hilal Ali, Shah, Karna, Al-Futaisi, Abdullah, Al-Zakwani, Ibrahim, Banerjee, Yajnavalka
Formato: Artigo
Idioma:Inglês
Publicado: OMJ 2013
Assuntos:
Case Report
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC3562979/
https://ncbi.nlm.nih.gov/pubmed/23386946
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5001/omj.2013.11
Tags: Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!

Títulos similares