Enamel defects in Acp4 R110C/R110C mice and human ACP4 mutations
Enamel defects in Acp4 R110C/R110C mice and human ACP4 mutations
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England: Nature Portfolio
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English
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England: Nature Portfolio
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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 pathogenesis of ACP4-...
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Enamel defects in Acp4 R110C/R110C mice and human ACP4 mutations
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TN_cdi_doaj_primary_oai_doaj_org_article_b1ed9c32d099421cbc3e834f910de5b2
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_b1ed9c32d099421cbc3e834f910de5b2
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E-ISSN
2045-2322
DOI
10.1038/s41598-022-20684-9
