A de novo mutation in ZMYND11, a candidate gene for 10p15.3 deletion syndrome, is associated with syndromic intellectual disability
- 1 November 2014
- journal article
- case report
- Published by Elsevier BV in European Journal of Medical Genetics
- Vol. 57 (11-12), 636-638
- https://doi.org/10.1016/j.ejmg.2014.09.002
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Structural and Functional Analysis of the DEAF-1 and BS69 MYND DomainsPLOS ONE, 2013
- Subtelomeric deletion of chromosome 10p15.3: Clinical findings and molecular cytogenetic characterizationAmerican Journal of Medical Genetics Part A, 2012
- De Novo Gene Disruptions in Children on the Autistic SpectrumNeuron, 2012
- BS69 undergoes SUMO modification and plays an inhibitory role in muscle and neuronal differentiationExperimental Cell Research, 2009