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Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa
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1998 (English)In: Science, ISSN 0036-8075, E-ISSN 1095-9203, Vol. 280, no 5370, p. 1753-1757Article in journal (Refereed) Published
Abstract [en]

Usher syndrome type IIa (OMIM 276901), an autosomal recessive disorder characterized by moderate to severe sensorineural hearing loss and progressive retinitis pigmentosa, maps to the long arm of human chromosome 1q41 between markers AFM268ZD1 and AFM144XF2. Three biologically important mutations in Usher syndrome type IIa patients were identified in a gene (USH2A) isolated from this critical region. The USH2A gene encodes a protein with a predicted size of 171.5 kilodaltons that has laminin epidermal growth factor and fibronectin type III motifs; these motifs are most commonly observed in proteins comprising components of the basal lamina and extracellular matrixes and in cell adhesion molecules.

Place, publisher, year, edition, pages
1998. Vol. 280, no 5370, p. 1753-1757
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Medical and Health Sciences
Research subject
Medicine
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URN: urn:nbn:se:oru:diva-10198DOI: 10.1126/science.280.5370.1753OAI: oai:DiVA.org:oru-10198DiVA: diva2:305540
Available from: 2010-03-24 Created: 2010-03-24 Last updated: 2017-12-12Bibliographically approved

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Möller, Claes

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