New insights on the roles of BMP signaling in bone-A review of recent mouse genetic studies
Author:
Publisher
Wiley
Subject
Clinical Biochemistry,Molecular Medicine,General Medicine,Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/biof.139/fullpdf
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3. A human chondrodysplasia due to a mutation in a TGF-beta superfamily member;Thomas;Nat. Genet.,1996
4. A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva;Shore;Nat. Genet.,2006
5. Duplications involving a conserved regulatory element downstream of BMP2 are associated with brachydactyly type A2;Dathe;Am. J. Hum. Genet.,2009
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