Enamel defects in Acp4R110C/R110C mice and human ACP4 mutations
Enamel defects in Acp4R110C/R110C mice and human ACP4 mutations
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Publisher
London: Nature Publishing Group UK
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Language
English
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Publisher
London: Nature Publishing Group UK
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Contents
Human
ACP4
(OMIM*606362) encodes a transmembrane protein that belongs to histidine acid phosphatase (ACP) family. Recessive mutations in
ACP4
cause non-syndromic hypoplastic amelogenesis imperfecta (AI1J, OMIM#617297). While ACP activity has long been detected in developing teeth, its functions during tooth development and the pathogene...
Alternative Titles
Full title
Enamel defects in Acp4R110C/R110C mice and human ACP4 mutations
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TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9526733
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9526733
Other Identifiers
ISSN
2045-2322
E-ISSN
2045-2322
DOI
10.1038/s41598-022-20684-9
