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Molecular diagnosis methods in familial hypercholesterolemia

Familial hypercholesterolemia (FH) is considered the genetic cause of coronary heart disease and ischemic stroke. FH is mainly an autosomal codominant pattern-based disorder and is primarily determined by point mutations within the low-density lipoprotein receptor, apolipoprotein B, and proprotein c...

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Detalles Bibliográficos
Autores principales:	Moldovan, Valeriu, Banescu, Claudia, Dobreanu, Minodora
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Kare Publishing 2020
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7222642/ https://www.ncbi.nlm.nih.gov/pubmed/32120369 http://dx.doi.org/10.14744/AnatolJCardiol.2019.95038

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