Periodontal disease and FAM20A mutations

• المؤلفون الرئيسيون: Kantaputra P., Bongkochwilawan C., Lubinsky M., Pata S., Kaewgahya M., Tong H., Ketudat Cairns J., Guven Y., Chaisrisookumporn N.
• التنسيق: دورية
• منشور في: 2017
• الوصول للمادة أونلاين: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85018909227&origin=inward; http://cmuir.cmu.ac.th/jspui/handle/6653943832/40341
• المؤسسة: Chiang Mai University

© 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...