Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/53295
Title: Root dentin anomaly and a PLG mutation
Authors: Napaporn Tananuvat
Pimlak Charoenkwan
Atsushi Ohazama
James R. Ketuda Cairns
Massupa Kaewgahya
Piranit Nik Kantaputra
Keywords: Biochemistry, Genetics and Molecular Biology
Medicine
Issue Date: 1-Jan-2014
Abstract: © 2014 Elsevier Masson SAS. We report a Thai girl affected with plasminogen deficiency, Type I. Ligneous conjunctivitis was first observed when she was one-month-old. The newly recognized findings include tapered incisor roots as a result of thin root dentin, generalized short tooth roots, and mandibular prognathism. Mutation analysis of PLG demonstrated homozygous c.1193G>A missense mutation. The parents were heterozygous for c.1193G>A mutation. The c.1193G>A mutation is novel and predicted to cause amino acid substitution p.Cys398Tyr. Thin root dentin in the patient who was affected with PLG mutation and immunolocalization of Plg during early root development in mice imply the role of plasminogen in root dentin formation.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84918834387&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/53295
ISSN: 18780849
17697212
Appears in Collections:CMUL: Journal Articles

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