Published in

Springer Nature [academic journals on nature.com], Molecular Psychiatry, 1(17), p. 4-7, 2011

DOI: 10.1038/mp.2011.95

Links

Tools

Export citation

Search in Google Scholar

CCDC22: a novel candidate gene for syndromic X-linked intellectual disability

Journal article published in 2011 by I. Voineagu, J. Voineagu, L. Huang, K. Winden, M. Lazaro, E. Haan, J. Nelson, J. McGaughran, Ls S. Nguyen, K. Friend, A. Hackett, M. Field, J. Gecz ORCID, D. Geschwind
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

Full text: Download

Green circle
Preprint: archiving allowed
Upload
Orange circle
Postprint: archiving restricted
Upload
Red circle
Published version: archiving forbidden
Policy details
Data provided by SHERPA/RoMEO

Abstract

Letter to the Editor: X-linked intellectual disability (XLID), defined as clinical ID combined with a pedigree consistent with X-linked inheritance, is a genetically heterogeneous condition that affects more than 10% of males with ID. Currently there are at least 92 genes known to cause XLID, 1-3 yet a large proportion of XLID cases remain unexplained, as each of the XLID genes identified so far only accounts for a small fraction (