WNT10B mutations associated with isolated dental anomalies

• Main Authors: P. N. Kantaputra, A. Hutsadaloi, M. Kaewgahya, W. Intachai, R. German, M. Koparal, C. Leethanakul, A. Tolun, J. R. Ketudat Cairns
• Format: Journal
• Published: 2018
• Subjects: Biochemistry, Genetics and Molecular Biology; Medicine
• Online Access: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85043235613&origin=inward; http://cmuir.cmu.ac.th/jspui/handle/6653943832/58264
• Institution: 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...