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...

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Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: OMJ 2013
Témata:
Case Report
On-line přístup: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
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