Author:
Kinoshita Yuka,Hori Michiko,Taguchi Manabu,Fukumoto Seiji
Funder
Ministry of Health, Labour and Welfare, Japan
Subject
Histology,Physiology,Endocrinology, Diabetes and Metabolism
Reference35 articles.
1. Unknown syndrome: microcephaly, hypoplastic nose, exophthalmos, gum hyperplasia, cleft palate, low set ears, and osteosclerosis;Raine;J Med Genet,1989
2. Mutations in FAM20C are associated with lethal osteosclerotic bone dysplasia (Raine syndrome), highlighting a crucial molecule in bone development;Simpson;Am J Hum Genet,2007
3. Mutations in FAM20C also identified in non-lethal osteosclerotic bone dysplasia;Simpson;Clin Genet,2009
4. Osteosclerotic bone dysplasia in siblings with a Fam20C mutation;Fradin;Clin Genet,2011
5. Exome sequencing reveals FAM20c mutations associated with fibroblast growth factor 23-related hypophosphatemia, dental anomalies, and ectopic calcification;Rafaelsen;J Bone Miner Res,2013
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