GREMLIN 2 mutations and dental anomalies

• المؤلفون الرئيسيون: P. N. Kantaputra, M. Kaewgahya, A. Hatsadaloi, P. Vogel, K. Kawasaki, A. Ohazama, J. R. Ketudat Cairns
• التنسيق: دورية
• منشور في: 2018
• الموضوعات: Agricultural and Biological Sciences
• الوصول للمادة أونلاين: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84948390495&origin=inward; http://cmuir.cmu.ac.th/jspui/handle/6653943832/44900

© International & American Associations for Dental Research 2015. Isolated or nonsyndromic tooth agenesis or hypodontia is the most common human malformation. It has been associated with mutations in MSX1, PAX9, EDA, AXIN2, EDAR, EDARADD, and WNT10A. GREMLIN 2 (GREM2) is a strong bone morphoge...