A 3-base pair deletion, c.9711_9713del, in DMD results in intellectual disability without muscular dystrophy

Brouwer, A.P.M. de; Nabuurs, S.B.; Verhaart, I.E.C.; Oudakker, A.R.; Hordijk, R.; Yntema, H.G.; ... ; Kleefstra, T. (2014)

Article / Letter to editor

• DMD
• dystrophin
• X-linked intellectual disability
• MRX85
• locus
• Dp71

• All authors: Brouwer, A.P.M. de; Nabuurs, S.B.; Verhaart, I.E.C.; Oudakker, A.R.; Hordijk, R.; Yntema, H.G.; Hordijk-Hos, J.M.; Voesenek, K.; Vries, B.B.A. de; Essen, T. van; Chen, W.; Hu, H.; Chelly, J.; Dunnen, J.T. den; Kalscheuer, V.M.; Aartsma-Rus, A.M.; Hamel, B.C.J.; Bokhoven, H. van; Kleefstra, T.
• Date: 2014-04-30
• Journal: European Journal of Human Genetics
• Volume: 22
• Issue: 4
• Pages: 480 - 485
• DOI: doi:10.1038/ejhg.2013.169