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Mitochondrion ; 11(5): 729-34, 2011 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-21645648

RESUMEN

Mitochondrial DNA (mtDNA) mutations have been implicated in various age-related diseases. To further clarify the role of mtDNA variants in age-related hearing impairment (ARHI), we determined the DNA sequence of the entire mitochondrial genome of 400 individuals using the Affymetrix Human Mitochondrial Resequencing Array. These were the 200 worst hearing and the 200 best hearing from a collection of 947 Belgian samples. We performed association tests with individual mitochondrial variants, comparison of the mutation load, and association with European haplogroups and their interaction with environmental risk factors. We also tested the influence of rare variants on ARHI. None of these tests showed any association with ARHI.


Asunto(s)
Herencia , Mitocondrias/genética , Mutación , Presbiacusia/genética , Anciano , Bélgica/epidemiología , Genes Mitocondriales , Estudios de Asociación Genética , Haplotipos , Humanos , Persona de Mediana Edad , Fenotipo , Polimorfismo de Nucleótido Simple , Presbiacusia/epidemiología , Factores de Riesgo , Análisis de Secuencia de ADN , Estadísticas no Paramétricas
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