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

Date
2016
Author
Koruyucu, M.
Gencay, K.
HYUN, H-K
LEE, Z. H.
KIM, J-W
Seymen, Figen
Kasimoglu, Y.
KIM, Y-J
SHIN, T. J.
Metadata
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Abstract
ObjectiveTo identify the molecular genetic aetiology of a family with autosomal dominant amelogenesis imperfecta (AI).
URI
http://hdl.handle.net/20.500.12627/55735
https://doi.org/10.1111/odi.12439
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