Contribution of Chromosome 1q21‐q23 to Familial Combined Hyperlipidemia in Mexican Families

Summary Familial combined hyperlipidemia (FCHL) is the most common familial dyslipidemia, with a prevalence of 1‐2% in the general population. A major locus for FCHL has been mapped to chromosome 1q21‐q23 in Finnish, Chinese, German and US families. We studied seven extended Mexican families with 15...

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Veröffentlicht in:	Annals of human genetics 2004-09, Vol.68 (5), p.419-427
Hauptverfasser:	Huertas‐Vázquez, A., del Rincón, J. P., Canizales‐Quinteros, S., Riba, L., Vega‐Hernández, G., Ramírez‐Jiménez, S., Aurón‐Gómez, M., Gómez–Pérez, F. J., Aguilar‐Salinas, C. A., Tusié‐Luna, M. T.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult candidate genes Cholesterol Chromosome 1 Chromosomes, Human, Pair 1 - genetics Data processing Dyslipidemia Female Genetic Linkage Genetic Predisposition to Disease Humans Hyperlipidemia Hyperlipidemia, Familial Combined - genetics Linkage analysis lipid metabolism Male Mexico Middle Aged Pedigree Phenotype Susceptibility Triglycerides Triglycerides - blood
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