Periodontal disease and FAM20A mutations

Periodontal disease and FAM20A mutations

© 2017 The Japan Society of Human Genetics All rights reserved. Enamel-renal-gingival syndrome (ERGS; OMIM #204690), a rare autosomal recessive disorder caused by mutations in FAM20A, is characterized by nephrocalcinosis, nephrolithiasis, amelogenesis imperfecta, hypoplastic type, gingival fibromato...

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Main Authors: Piranit Nik Kantaputra, Chotika Bongkochwilawan, Mark Lubinsky, Supansa Pata, Massupa Kaewgahya, Huei Jinn Tong, James R. Ketudat Cairns, Yeliz Guven, Nipon Chaisrisookumporn
Format: Journal
Published: 2018
Subjects:
Biochemistry, Genetics and Molecular Biology
Medicine
Online Access:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85018909227&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/56743
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Institution: Chiang Mai University

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https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85018909227&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/56743

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