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Human Molecular Genetics
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Human Molecular Genetics
Article . 1995 . Peer-reviewed
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A human recessive neurosensory nonsyndromic hearing impairment locus is a potential homologue of the murine deafness (dn) locus

Authors: Jain, Pawan K.; Fukushima, Kunihiro; Deshmukh, Dilip; Ramesh, Arabandi; Thomas, Elizabeth; Lalwani, Anil K.; Kumar, Subrinder; +8 Authors

A human recessive neurosensory nonsyndromic hearing impairment locus is a potential homologue of the murine deafness (dn) locus

Abstract

A locus for recessive neurosensory nonsyndromic hearing impairment maps to chromosome 9q13-q21 in two regionally separate consanguineous families from India. Each family demonstrates a LOD score greater than 4.5 to this region. D9S15, tightly linked to the Friedreich's ataxia locus, a region that has been defined with over 1 Mb of YAC contig information and several expressed sequences, is one of the flanking markers. In mice, the deafness (dn) locus maps to mouse chromosome 19 and flanking loci are syntenic to human chromosome 9q11-q21. The dn mouse is a potential model for the hearing impairment found in both these families.

Keywords

Male, Consanguinity, Hearing Loss, Sensorineural, Chromosome Mapping, Humans, Female, Genes, Recessive, Chromosomes, Human, Pair 9, Pedigree

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popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
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influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
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impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
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