Unexpected identification of a recurrent mutation in the DLX3 gene causing amelogenesis imperfecta

Date
2016
Author
Kım, Y-J
Hyun, H-K
Shın, T. J.
Lee, Z. H.
Kım, J-W
Kasimoglu, Y.
Koruyucu, M.
Gencay, K.
Seymen, Figen
Metadata
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Abstract
ObjectiveTo identify the molecular genetic aetiology of a family with autosomal dominant amelogenesis imperfecta (AI).
URI
10.1111/odi.12439
http://hdl.handle.net/20.500.12627/1050
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