WNT10B mutations associated with isolated dental anomalies

• المؤلفون الرئيسيون: P. N. Kantaputra, A. Hutsadaloi, M. Kaewgahya, W. Intachai, R. German, M. Koparal, C. Leethanakul, A. Tolun, J. R. Ketudat Cairns
• التنسيق: دورية
• منشور في: 2018
• الوصول للمادة أونلاين: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85043235613&origin=inward; http://cmuir.cmu.ac.th/jspui/handle/6653943832/48398
• المؤسسة: Chiang Mai University

© 2018 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd Isolated hypodontia is the most common human malformation. It is caused by heterozygous variants in various genes, with heterozygous WNT10A variants being the most common cause. WNT10A and WNT10B are paralogs that likely ev...