LOCALIZATION OF A GENE FOR NON-SYNDROMIC HEARING-LOSS (DFNA5) TO CHROMOSOME 7P15

Citation
G. Vancamp et al., LOCALIZATION OF A GENE FOR NON-SYNDROMIC HEARING-LOSS (DFNA5) TO CHROMOSOME 7P15, Human molecular genetics, 4(11), 1995, pp. 2159-2163
Citations number
34
Categorie Soggetti
Genetics & Heredity",Biology
Journal title
ISSN journal
09646906
Volume
4
Issue
11
Year of publication
1995
Pages
2159 - 2163
Database
ISI
SICI code
0964-6906(1995)4:11<2159:LOAGFN>2.0.ZU;2-Z
Abstract
Progressive hearing loss affects approximately 50% of the elderly by t he age of 80, and is most likely caused by an interaction of genetic a nd environmental factors. Identification of the genes responsible for hereditary hearing loss is therefore important. Families with pure gen etic degenerative hearing disorders may be helpful as the same genes m ay be also involved in age-related hearing Toss in general. In this st udy we have performed a genome search in an extended Dutch family with autosomal dominant progressive hearing loss starting in the high freq uencies. The gene causing hearing loss in this family was localized to the short arm of chromosome 7, in a 15 cM interval between markers D7 S493 and D7S632.