Citations for
1FGFR2, LADD1, ALSG, FGF10
Structural basis for reduced FGFR2 activity in LADD syndrome: Implications for FGFR autoinhibition and activation.
Lew ED, Bae JH, Rohmann E, Wollnik B, Schlessinger J.
Proc Natl Acad Sci U S A 104(50):19802-7. Epub 2007 Dec 3. 2007
2FGFR2, FGFR3, FGF10, LADD1, LADD2, LADD3
Mutations in different components of FGF signaling in LADD syndrome.
Rohmann E, Brunner HG, Kayserili H, Uyguner O, Nurnberg G, Lew ED, Dobbie A, Eswarakumar VP, Uzumcu A, Ulubil-Emeroglu M, Leroy JG, Li Y, Becker C, Lehnerdt K, Cremers CW, Yuksel-Apak M, Nurnberg P, Kubisch C, Schlessinger J, van Bokhoven H, Wollnik B.
Nat Genet 38(4):414-7. Epub 2006 Feb 26. 2006
3LADD1, FGFR2, LADD2, FGFR3, LADD3, FGF10
Still more from FGFR: LADD syndrome caused by different mutations in FGFR and their ligands.
Timmerman M.
Clin Genet 70(1):17-9. No abstract available. 2006