Matches in Nanopublications for { ?s ?p "[Amelogenin with a proline 41 to threonine mutation (P41T) is hydrolyzed at a lower rate by matrix metalloproteinase 20 (MMP20), resulting in an inherited tooth enamel defect, amelogenesis imperfecta (AI).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP391314.RAX5WaOLzMTreZm4gqHC8ZC0VlSQPm-s4pbdjW0F8Uss4130_assertion description "[Amelogenin with a proline 41 to threonine mutation (P41T) is hydrolyzed at a lower rate by matrix metalloproteinase 20 (MMP20), resulting in an inherited tooth enamel defect, amelogenesis imperfecta (AI).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP391314.RAX5WaOLzMTreZm4gqHC8ZC0VlSQPm-s4pbdjW0F8Uss4130_provenance.