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Genes and Related Proteins Involved in Amelogenesis Imperfecta

✍ Scribed by Stephanopoulos, G.; Garefalaki, M.-E.; Lyroudia, K.


Book ID
124069155
Publisher
International and American Association of Dental Research
Year
2005
Tongue
English
Weight
684 KB
Volume
84
Category
Article
ISSN
0022-0345

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Amelogenesis imperfecta (AI) is a genetically and clinically heterogeneous group of inherited dental enamel defects without any other nonoral symptoms. Recently, a disease-causing nonsense mutation (c.406C>T) in a novel gene, FAM20A, was identified in a large consanguineous family affected by AI wit