TY - JOUR
T1 - CCDC22
T2 - A novel candidate gene for syndromic X-linked intellectual disability
AU - Voineagu, I.
AU - Huang, L.
AU - Winden, K.
AU - Lazaro, M.
AU - Haan, E.
AU - Nelson, J.
AU - McGaughran, J.
AU - Nguyen, L. S.
AU - Friend, K.
AU - Hackett, A.
AU - Field, M.
AU - Gecz, J.
AU - Geschwind, D.
N1 - Funding Information:
1Program in Neurogenetics and Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, CA, USA; 2Department of Genetics Medicine, SA Pathology, Adelaide, SA, Australia; 3Institute of Reproductive and Stem Cell Engineering, Central South University, Changsha, China; 4South Australian Clinical Genetics Service, SA Pathology, Adelaide, SA, Australia; 5Genetic Services of Western Australia, King Edward Memorial Hospital, Perth, WA, Australia; 6Genetic Health Queensland, Royal Brisbane and Women’s Hospital, Brisbane, QLD, Australia; 7University of Queensland, Brisbane, QLD, Australia; 8Department of Pediatrics, The University of Adelaide, Adelaide, SA, Australia; 9The GOLD Service, Hunter Genetics, Waratah, NSW, Australia; 10Women’s and Children’s Health Research Institute, North Adelaide, SA, Australia; 11School of Molecular and Biomedical Sciences, The University of Adelaide, Adelaide, SA, Australia and 12These authors contributed equally to this work E-mail: [email protected]
PY - 2012/1
Y1 - 2012/1
UR - https://www.scopus.com/pages/publications/84855359260
U2 - 10.1038/mp.2011.95
DO - 10.1038/mp.2011.95
M3 - Letter
C2 - 21826058
AN - SCOPUS:84855359260
SN - 1359-4184
VL - 17
SP - 4
EP - 7
JO - Molecular psychiatry
JF - Molecular psychiatry
IS - 1
ER -