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

✍ Scribed by 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

Book ID: 113423030
Publisher: American Society of Human Genetics
Year: 2011
Tongue: English
Weight: 660 KB
Volume: 88
Category: Article
ISSN: 0002-9297
DOI: 10.1016/j.ajhg.2011.04.005

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