Association of RXR-Gamma Gene Variants with Familial Combined Hyperlipidemia: Genotype and Haplotype Analysis

Background. Familial combined hyperlipidemia (FCHL), the most common genetic form of hyperlipdemia, is characterized by a strong familial clustering and by premature coronary heart disease. The FCHL locus has been mapped to human chromosome 1q21-q23. This region includes the retinoid X receptor gamm...

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Main Authors: Sentinelli, Federica, Minicocci, Ilenia, Montali, Anna, Nanni, Luisa, Romeo, Stefano, Incani, Michela, Cavallo, M. Gisella, Lenzi, Andrea, Arca, Marcello, Baroni, Marco G.
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi Publishing Corporation 2013
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3810489/
https://ncbi.nlm.nih.gov/pubmed/24222859
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2013/517943
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