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: | , , , , , , , , |
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Format: | Journal |
Published: |
2017
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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 |