Genetic Analysis of Iranian Patients with Familial Hypercholesterolemia

BACKGROUND: Familial hypercholesterolemia (FH) is a frequent autosomal dominant disorder of lipoprotein metabolism. This disorder is generally caused by mutations in low-density lipoprotein receptor (LDLR), apolipoprotein B 100 (APOB), and proprotein convertase subtilisin/kexin type 9 (PCSK9) genes....

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Detalhes bibliográficos
Publicado no:Iran Biomed J
Main Authors: Ekrami, Mahdis, Torabi, Maryam, Ghafouri-Fard, Soudeh, Mowla, Javad, Soltani, Bahram Mohammad, Hashemi-Gorji, Feyzollah, Mohebbi, Zahra, Miryounesi, Mohammad
Formato: Artigo
Idioma:Inglês
Publicado em: Pasteur Institute 2018
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5786657/
https://ncbi.nlm.nih.gov/pubmed/28734274
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.22034/ibj.22.2.117
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