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Orphanet journal of rare diseases, v.3, 2008년, pp.31 - 31
Barron, Martin J (Faculty of Life Sciences and Dental School, Michael Smith Building, University of Manchester, Oxford Road, Manchester, M13 9PT, UK) , McDonnell, Sinead T (Dental School, University of Manchester, Oxford Road, Manchester M13 9PT, UK) , MacKie, Iain (Dental School, University of Manchester, Oxford Road, Manchester M13 9PT, UK) , Dixon, Michael J (Faculty of Life Sciences and Dental School, Michael Smith Building, University of Manchester, Oxford Road, Manchester, M13 9PT, UK)
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The hereditary dentine disorders, dentinogenesis imperfecta (DGI) and dentine dysplasia (DD), comprise a group of autosomal dominant genetic conditions characterised by abnormal dentine structure affecting either the primary or both the primary and secondary dentitions. DGI is reported to have an in...
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