Literature for peptidase M10.019: matrix metallopeptidase-20

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2021
1. Nikolopoulos,G., Smith,C.E.L., Poulter,J.A., Murillo,G., Silva,S., Lamb,T., Berry,I.R., Brown,C.J., Day,P.F., Soldani,F., Al-Bahlani,S., Harris,S.A., O'Connell,M.J., Inglehearn,C.F. and Mighell,A.J.
   Spectrum of pathogenic variants and founder effects in amelogenesis imperfecta associated with MMP20
   Hum Mutat PubMed  Europe PubMed DOI  M
2013
2. Wang,S.K., Hu,Y., Simmer,J.P., Seymen,F., Estrella,N.M.R.P., Pal,S., Reid,B.M., Yildirim,M., Bayram,M., Bartlett,J.D. and Hu,J.C.C.
   Novel KLK4 and MMP20 mutations discovered by whole-exome sequencing
   J Dent Res92, 266-271. PubMed  Europe PubMed DOI  M
2010
3. Lee,S.K., Seymen,F., Kang,H.Y., Lee,K.E., Gencay,K., Tuna,B. and Kim,J.W.
   MMP20 hemopexin domain mutation in amelogenesis imperfecta
   J Dent Res89, 46-50. PubMed  Europe PubMed DOI  M
2008
4. Papagerakis,P., Lin,H.K., Lee,K.Y., Hu,Y., Simmer,J.P., Bartlett,J.D. and Hu,J.C.
   Premature stop codon in MMP20 causing amelogenesis imperfecta
   J Dent Res87, 56-59. PubMed  Europe PubMed DOI  M
2005
5. Kim,J.W., Simmer,J.P., Hart,T.C., Hart,P.S., Ramaswami,M.D., Bartlett,J.D. and Hu,J.C.
   MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta
   J Med Genet42, 271-275. PubMed  Europe PubMed DOI  M
6. Ozdemir,D., Hart,P.S., Ryu,O.H., Choi,S.J., Ozdemir-Karatas,M., Firatli,E., Piesco,N. and Hart,T.C.
   MMP20 active-site mutation in hypomaturation amelogenesis imperfecta
   J Dent Res84, 1031-1035. PubMed  Europe PubMed DOI  M