Evidence for regulation of amelogenin ge
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Petros Papagerakis; Dominique Hotton; Frederic Lezot; Steve Brookes; William Bon
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Article
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2000
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John Wiley and Sons
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English
β 437 KB
π 1 views
The unique hereditary enamel defect clearly related to the disturbance of one enamel matrix protein is X-linked amelogenesis imperfecta (AI), in which several mutations of amelogenin gene have been identified. The clinical phenotype of many of these subjects shows similarities with enamel defects re