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Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11
Örebro University, School of Health and Medical Sciences.ORCID iD: 0000-0001-6557-6359
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1992 (English)In: Genomics, ISSN 0888-7543, E-ISSN 1089-8646, Vol. 14, no 4, 988-994 p.Article in journal (Refereed) Published
Abstract [en]

Usher syndrome is the most commonly recognized cause of combined visual and hearing loss in technologically developed countries. There are several different types and all are inherited in an autosomal recessive manner. There may be as many as five different genes responsible for at least two closely related phenotypes. The nature of the gene defects is unknown, and positional cloning strategies are being employed to identify the genes. This is a report of the localization of one gene for Usher syndrome type I to chromosome 11q, probably distal to marker D11S527. Another USH1 gene had been previously localized to chromosome 14q, and this second localization establishes the existence of a new and independent locus for Usher syndrome.

Place, publisher, year, edition, pages
1992. Vol. 14, no 4, 988-994 p.
National Category
Medical and Health Sciences
Research subject
Medicine
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URN: urn:nbn:se:oru:diva-10010DOI: 10.1016/S0888-7543(05)80121-1OAI: oai:DiVA.org:oru-10010DiVA: diva2:303747
Available from: 2010-03-15 Created: 2010-03-15 Last updated: 2016-12-16Bibliographically approved

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