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Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome

Author:

James O'Sullivan,Carolina C. Bitu,Sarah B. Daly,Jill E. Urquhart,Martin J. Barron,Sanjeev S. Bhaskar,Hercilio Martelli-Júnior,Pedro Eleuterio dos Santos Neto,Maria A. Mansilla,Jeffrey C. Murray,Ricardo D. Coletta,Graeme C.M. Black,Michael J. Dixon

Publication:

The American Journal of Human Genetics

Publisher:

Elsevier

Date:

13 May 2011

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