Autosomal recessive gingival hyperplasia and dental anomalies caused by a 29-base pair duplication in the FAM20A gene
- 23 May 2013
- journal article
- other
- Published by Springer Science and Business Media LLC in Journal of Human Genetics
- Vol. 58 (8), 566-567
- https://doi.org/10.1038/jhg.2013.44
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
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- Novel FAM20A mutations in hypoplastic amelogenesis imperfectaHuman Mutation, 2011
- Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia SyndromeAmerican Journal of Human Genetics, 2011
- Defining a New Candidate Gene for Amelogenesis Imperfecta: From Molecular Genetics to BiochemistryBiochemical Genetics, 2010
- Mutations in FAM20C Are Associated with Lethal Osteosclerotic Bone Dysplasia (Raine Syndrome), Highlighting a Crucial Molecule in Bone DevelopmentAmerican Journal of Human Genetics, 2007
- FAM20: an evolutionarily conserved family of secreted proteins expressed in hematopoietic cellsBMC Genomics, 2005