Low bone mineral density in achondroplasia and hypochondroplasia
Author:
Affiliation:
1. Department of Orthopaedic Surgery; Nagoya University Graduate School of Medicine; Nagoya Japan
Publisher
Wiley
Subject
Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/ped.12890/fullpdf
Reference22 articles.
1. The population-based prevalence of achondroplasia and thanatophoric dysplasia in selected regions of the US;Waller;Am. J. Med. Genet. A,2008
2. A common FGFR3 gene mutation in hypochondroplasia;Prinos;Hum. Mol. Genet.,1995
3. Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia;Shiang;Cell,1994
4. Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia;Rousseau;Nature,1994
5. Gain-of-function mutation in FGFR3 in mice leads to decreased bone mass by affecting both osteoblastogenesis and osteoclastogenesis;Su;Hum. Mol. Genet.,2010
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