Genome Research · 1995 · 56 citations · 14 references
Life SciencesGeneticsMolecular GeneticsHearing ScienceHuman GeneticsMedical GeneticsCochlear DisordersGenetic DisordersGenetic SyndromesHearing ImpairmentHearing LossRare Disease GeneticsAutosomal Recessive InheritanceGenetic Inner Ear DisordersGenomic Dna AnalysisHearing Loss EtiologyNon-syndromic Hearing LossPooled Genotyping
Autosomal recessive nonsyndromic hearing loss (ARNSHL) is the most common form of congenitally acquired inherited hearing impairment. Although numerous loci are believed to exist, only five have been identified. Using a pooled genomic DNA screening strategy, we have identified a sixth locus, DFNB6, on 3p in the interval bounded by D3S1619 and D3S1766.
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