research data . Dataset . 2016

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

Harrison, Sean; Lewis, Sarah; Hall, Amanda; Vuckovic, Dragana; Girotto, Giorgia; Martin, Richard; Adams, Josephine;
  • Published: 15 Dec 2016
  • Publisher: Figshare
Abstract
Abstract Background The 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 h
Subjects
Medical Subject Headings: otorhinolaryngologic diseases
free text keywords: Medicine, Genetics, Neuroscience, Physiology, 69999 Biological Sciences not elsewhere classified, 111714 Mental Health, Mental Health
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figshare
Dataset . 2016
Provider: Datacite
figshare
Dataset . 2016
Provider: Datacite
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research data . Dataset . 2016

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

Harrison, Sean; Lewis, Sarah; Hall, Amanda; Vuckovic, Dragana; Girotto, Giorgia; Martin, Richard; Adams, Josephine;