首页> 美国卫生研究院文献>BMC Medical Genomics >Association of SNPs in LCP1 and CTIF with hearing in 11 year old children: Findings from the Avon Longitudinal Study of Parents and Children (ALSPAC) birth cohort and the G-EAR consortium
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Association of SNPs in LCP1 and CTIF with hearing in 11 year old children: Findings from the Avon Longitudinal Study of Parents and Children (ALSPAC) birth cohort and the G-EAR consortium

机译:LCP1和CTIF中SNP与11岁儿童的听力的关联:雅芳父母和儿童纵向研究(ALSPAC)出生队列和G-EAR联合会的发现

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摘要

BackgroundThe genetic basis of hearing loss in humans is relatively poorly understood. In recent years, experimental approaches including laboratory studies of early onset hearing loss in inbred mouse strains, or proteomic analyses of hair cells or hair bundles, have suggested new candidate molecules involved in hearing function. However, the relevance of these genes/gene products to hearing function in humans remains unknown. We investigated whether single nucleotide polymorphisms (SNPs) in the human orthologues of genes of interest arising from the above-mentioned studies correlate with hearing function in children.
机译:背景技术人类对听力损失的遗传基础了解甚少。近年来,包括对近交小鼠品系的早期发作性听力损失进行实验室研究或对毛细胞或发束进行蛋白质组学分析在内的实验方法已提出了涉及听力功能的新候选分子。然而,这些基因/基因产物与人类听力功能的相关性仍然未知。我们调查了由上述研究引起的人类感兴趣基因直向同源物中的单核苷酸多态性(SNP)是否与儿童的听力功能相关。

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