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EMQN Best Practice guidelines for diagnostic testing of mutations causing non-syndromic hearing impairment at the DFNB1 locus.
2013 (English)In: European Journal of Human Genetics, ISSN 1018-4813, E-ISSN 1476-5438, Vol. 21, no 11, 1325-1329 p.Article in journal (Refereed) Published
Place, publisher, year, edition, pages
2013. Vol. 21, no 11, 1325-1329 p.
National Category
Medical Genetics Basic Medicine
Research subject
Clinical Genetics
URN: urn:nbn:se:uu:diva-223937DOI: 10.1038/ejhg.2013.83OAI: oai:DiVA.org:uu-223937DiVA: diva2:714489

Collaborator: Marie-Louise Bondeson, Institutionen för immunologi, genetik och patologi, Medicinsk genetik; Uppsala, Sweden

Available from: 2014-04-28 Created: 2014-04-28 Last updated: 2014-08-11Bibliographically approved

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