A de novo mutation in ZMYND11, a candidate gene for 10p15.3 deletion syndrome, is associated with syndromic intellectual disability.

Autor: Cobben JM; Dpt of Pediatrics and Clinical Genetics, AMC University Hospital, Amsterdam, The Netherlands; Dpt of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands. Electronic address: j.m.cobben@amc.uva.nl., Weiss MM; Dpt of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands., van Dijk FS; Dpt of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands., De Reuver R; Dpt of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands., de Kruiff C; Dpt of Pediatrics and Clinical Genetics, AMC University Hospital, Amsterdam, The Netherlands., Pondaag W; Dpt of Neurosurgery, LUMC University Hospital, Leiden, The Netherlands., Hennekam RC; Dpt of Pediatrics and Clinical Genetics, AMC University Hospital, Amsterdam, The Netherlands., Yntema HG; Dpt of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.

Publikováno v: European journal of medical genetics [Eur J Med Genet] 2014 Nov-Dec; Vol. 57 (11-12), pp. 636-8. Date of Electronic Publication: 2014 Sep 30.