| 1 | AIH1, AIH2, AIPH1, AIPH2, AMELX, ENAM, KLK4, MMP20
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| Human and mouse enamel phenotypes resulting from mutation or altered expression of AMEL, ENAM, MMP20 and KLK4.
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| Wright JT, Hart TC, Hart PS, Simmons D, Suggs C, Daley B, Simmer J, Hu J, Bartlett JD, Li Y, Yuan ZA, Seow WK, Gibson CW.
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| Cells Tissues Organs 189(1-4):224-9. Epub 2008 Aug 19. 2009
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| 2 | AI1C, AIH1, AIH2, AIH3, AIHHT, AIPH1, AIPH2, AMELX, AXIN1, DD2, DGI1, DLX3, DSPP, ENAM, FTA1, FTACC, KLK4, MMP20, MSX1, OLD, PAX9, STHAG5, ZNF22
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| The genetic basis of inherited anomalies of the teeth. Part 1: clinical and molecular aspects of non-syndromic dental disorders.
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| Bailleul-Forestier I, Molla M, Verloes A, Berdal A.
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| Eur J Med Genet 51(4):273-91. Epub 2008 Mar 26. Review.
2008
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| 3 | AIPH1, MMP20, AIPH2
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| MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta.
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| Kim JW, Simmer JP, Hart TC, Hart PS, Ramaswami MD, Bartlett JD, Hu JC.
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| J Med Genet 42(3):271-5. No abstract available. 2005
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| 4 | AIPH1, KLK4
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| Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta.
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| Hart PS, Hart TC, Michalec MD, Ryu OH, Simmons D, Hong S, Wright JT.
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| J Med Genet 41(7):545-9. No abstract available. 2004
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