Molecular pathology of the fibroblast growth factor family
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.21067/fullpdf
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3. Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23;ADHR Consortium;Nat Genet,2000
4. Role of heparan sulfate as a tissue-specific regulator of FGF-4 and FGF receptor recognition;Allen;J Cell Biol,2001
5. Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 (FGF3);Alsmadi;Eur J Hum Genet,2009
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