Back to Search Start Over

Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two families

Authors :
Coucke, Paul
Camp, Guy van
Djoyodiharjo, Bulantrisna
Smith, Shelley D.
Frants, Rune R.
Padberg, George W.
Darby, John K.
Huizing, Egbert H.
Cremers, Cor W.R.J.
Kimberling, William J.
Oostra, Ben A.
Heyning, Paul H. van de
Willems, Patrick J.
Source :
The New England Journal of Medicine. August 18, 1994, Vol. v331 Issue n7, p425, 7 p.
Publication Year :
1994

Abstract

Hereditary hearing loss that begins early in life may be traced to a gene on chromosome 1p. Researchers studied a large Indonesian family with hereditary, progressive deafness. DNA samples were analyzed from 15 family members with hearing loss. A genetic-linkage analysis was performed to pinpoint the location of the gene for deafness. The gene was localized between D1S211 and D1S201 on chromosome 1p. Linkage analysis was then performed in American and Dutch families with hereditary hearing loss to determine if the same region on chromosome 1p was the location of the gene for deafness. In the American family, the gene was positioned on D1S255 on chromosome 1p. In the Dutch family, the gene for deafness was not located in the suspected region on chromosome 1p. Because the Indonesian and American families are of different ethnic groups, researchers suspect that the gene that causes deafness on chromosome 1p may be responsible for hereditary hearing loss in other families.

Details

ISSN :
00284793
Volume :
v331
Issue :
n7
Database :
Gale General OneFile
Journal :
The New England Journal of Medicine
Publication Type :
Academic Journal
Accession number :
edsgcl.15814766