نتایج جستجو برای: mmp20
تعداد نتایج: 76 فیلتر نتایج به سال:
Spectrum of pathogenic variants and founder effects in amelogenesis imperfecta associated with MMP20
amelogenesis imperfecta (ai) is a disorder of tooth development where there is an abnormal formation of enamel or the external layer of teeth. the aim of this study was to screen mutations in the four most important candidate genes, enam, klk4, mmp20 and fam83h responsible for amelogenesis imperfect.geneomic dna was isolated from five iranian families with 22 members affected with enamel malfor...
background: amelogenesis imperfecta (ai) is an inherited tooth disorder. despite the fact that up to now, several gene mutations in mmp20, enam, amelx and klk4 genes have been reported to be associated with ai, many other genes suggested to be involved. the main objective of this study was to find the mutations in three major candidate genes including mmp20, enam and klk4 responsible for ai f...
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