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HNO. 2009 Apr;57(4):371-6. doi: 10.1007/s00106-008-1832-9.

[A new gene locus for an autosomal-dominant non-syndromic hearing impairment (DFNA 33) is situated on chromosome 13q34-qter].

[Article in German]

Author information

1
Abteilung für Psychiatrie, Psychotherapie und Suchtmedizin, Kliniken Essen-Mitte, Essen.

Abstract

By investigation of a German family pedigree with non-syndromic hearing impairment of early onset and autosomal-dominant mode of inheritance, linkage to known DFNA loci was excluded, and the existence of a new locus (DFNA33) was revealed. In a subsequent genomic scan the phenotype was mapped to a 6 cM interval on chromosome 13q34-qter. A maximum two-point lod score of 2.96 was obtained for the marker D13S285 with a maximum lod score in the multipoint analysis of 3.28 at 124.56 cM.

PMID:
19183916
DOI:
10.1007/s00106-008-1832-9
[Indexed for MEDLINE]

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