LAF4 maps to mouse Chromosome 1 and human Chromosome 2q11.2-q12

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A novel locus for autosomal dominant non-syndromic deafness, DFNA53, maps to chromosome 14q11.2-q12.

BACKGROUND Non-syndromic hearing loss is among the most genetically heterogeneous traits known in humans. To date, at least 50 loci for autosomal dominant non-syndromic sensorineural hearing loss (ADNSSHL) have been identified by linkage analysis. OBJECTIVE To report the mapping of a novel autosomal dominant deafness locus on the long arm of chromosome 14 at 14q11.2-q12, DFNA53, in a large mu...

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ژورنال

عنوان ژورنال: Mammalian Genome

سال: 1996

ISSN: 0938-8990,1432-1777

DOI: 10.1007/s003359900137