Mouse Dspp frameshift model of human dentinogenesis imperfecta
Mouse Dspp frameshift model of human dentinogenesis imperfecta
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Author / Creator
Publisher
London: Nature Publishing Group UK
Journal title
Language
English
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Publication information
Publisher
London: Nature Publishing Group UK
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Contents
Non-syndromic inherited defects of tooth dentin are caused by two classes of dominant negative/gain-of-function mutations in dentin sialophosphoprotein (
DSPP
): 5′ mutations affecting an N-terminal targeting sequence and 3′ mutations that shift translation into the − 1 reading frame.
DSPP
defects cause an overlapping spectrum of phenot...
Alternative Titles
Full title
Mouse Dspp frameshift model of human dentinogenesis imperfecta
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TN_cdi_doaj_primary_oai_doaj_org_article_8cc6c2e7bcd84aac8371c3b57be3059c
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_8cc6c2e7bcd84aac8371c3b57be3059c
Other Identifiers
ISSN
2045-2322
E-ISSN
2045-2322
DOI
10.1038/s41598-021-00219-4
