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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Detalles Bibliográficos
Autores principales: Sentinelli, Federica, Minicocci, Ilenia, Montali, Anna, Nanni, Luisa, Romeo, Stefano, Incani, Michela, Cavallo, M. Gisella, Lenzi, Andrea, Arca, Marcello, Baroni, Marco G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3810489/
https://www.ncbi.nlm.nih.gov/pubmed/24222859
http://dx.doi.org/10.1155/2013/517943

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3810489/
https://www.ncbi.nlm.nih.gov/pubmed/24222859
http://dx.doi.org/10.1155/2013/517943

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