Overlapping microdeletions involving 15q22.2 narrow the critical region for intellectual disability to NARG2 and RORA

Yamamoto, T.; Mencarelli, M.A.; Marco, C. di; Mucciolo, M.; Vascotto, M.; Balestri, P.; ... ; Mari, F. (2014)

Article / Letter to editor

• 15q22.2
• Microdeletion
• Intellectual disability
• Epilepsy NMDA receptor
• regulated 2 (NARG2)
• RAR-related orphan receptor A (RORA)
• Forkhead box B1 (FOXB1)

• All authors: Yamamoto, T.; Mencarelli, M.A.; Marco, C. di; Mucciolo, M.; Vascotto, M.; Balestri, P.; Gerard, M.; Mathieu-Dramard, M.; Andrieux, J.; Breuning, M.; Hoffer, M.J.V.; Ruivenkamp, C.A.L.; Shimada, S.; Sangu, N.; Shimojima, K.; Umezu, R.; Kawame, H.; Matsuo, M.; Saito, K.; Renieri, A.; Mari, F.
• Date: 2014-03-31
• Journal: European Journal of Medical Genetics
• Volume: 57
• Issue: 4
• Pages: 163 - 168
• DOI: doi:10.1016/j.ejmg.2014.02.001