Enamel Defects in the Alpl- /- murine Model of Infantile Hypophosphatasia
Author:
Affiliation:
1. Nihon University Graduate School of Dentistry at Matsudo, Pediatric Dentistry, Matsudo, Chiba 271-8587, Japan
2. Department of Pediatric Dentistry, Nihon University School of Dentistry at Matsudo, Matsudo, Chiba 271-8587, Japan
Publisher
Nihon University School of Dentistry at Matsudo Research Institute of Oral Science
Link
https://www.jstage.jst.go.jp/article/ijoms/15/3-4/15_126/_pdf
Reference48 articles.
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2. 2. Mornet E: Hypophosphatasia. Orphanet J Rare Dis, 2: 40,2007.
3. 3. Wei KW, Xuan K, Liu YL, Fang J, Ji K, Wang X, Jin Y,Watanabe S, Watanabe K, Ojihara T: Clinical, pathological and genetic evaluations of Chinese patients with autosomal-dominant hypophosphatasia. Arch Oral Biol, 55: 1017-1023, 2010.
4. 4. McKee MD, Hoac B, Addison WN, Barros NM, Millán JL, Chaussain C: Extracellular matrix mineralization in periodon tal tissues: Noncollagenous matrix proteins, enzymes, and relationship to hypophosphatasia and X-linked hypophosphatemia. Periodontol 2000, 63: 102-122, 2013.
5. 5. Bloch-Zupan A: Hypophosphatasia: diagnosis and clinical signs - a dental surgeon perspective. Int J Paediatr Dent, 26: 426-438, 2016.
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