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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...
Autores principales: | Sentinelli, Federica, Minicocci, Ilenia, Montali, Anna, Nanni, Luisa, Romeo, Stefano, Incani, Michela, Cavallo, M. Gisella, Lenzi, Andrea, Arca, Marcello, Baroni, Marco G. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
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 |
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