The genetic spectrum of familial hypercholesterolemia in Pakistan

BACKGROUND: Familial hypercholesterolemia (FH) is an autosomal dominant disease caused by mutations in the genes coding for the low density lipoprotein receptor (LDLR), proprotein convertase subtilisin/kexin type-9 (PCSK9) or apo-lipoprotein B-100 (APOB). The aim of the present work was to determine...

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Detalles Bibliográficos
Autores principales: Ahmed, Waqas, Whittall, Ros, Riaz, Moeen, Ajmal, Muhammad, Sadeque, Ahmed, Ayub, Humaira, Qamar, Raheel, Humphries, Steve E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2013
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3701840/
https://www.ncbi.nlm.nih.gov/pubmed/23535506
http://dx.doi.org/10.1016/j.cca.2013.03.017

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3701840/
https://www.ncbi.nlm.nih.gov/pubmed/23535506
http://dx.doi.org/10.1016/j.cca.2013.03.017

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