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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Bibliographic Details
Main Authors: Kantaputra P., Bongkochwilawan C., Lubinsky M., Pata S., Kaewgahya M., Tong H., Ketudat Cairns J., Guven Y., Chaisrisookumporn N.
Format: Journal
Published: 2017
Online Access:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85018909227&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/40341
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Institution: Chiang Mai University
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