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

Voineagu, I., Huang, L., Winden, K., Lazaro, M., Haan, E., Nelson, J., McGaughran, J., Nguyen, L.S., Friend, K., Hackett, A., Field, M., Gecz, J. and Geschwind, D. (2012) CCDC22: a novel candidate gene for syndromic X-linked intellectual disability. Molecular Psychiatry, 17 1: 4-7. doi:10.1038/mp.2011.95


Author Voineagu, I.
Huang, L.
Winden, K.
Lazaro, M.
Haan, E.
Nelson, J.
McGaughran, J.
Nguyen, L.S.
Friend, K.
Hackett, A.
Field, M.
Gecz, J.
Geschwind, D.
Title CCDC22: a novel candidate gene for syndromic X-linked intellectual disability
Journal name Molecular Psychiatry   Check publisher's open access policy
ISSN 1359-4184
1476-5578
Publication date 2012-01-01
Year available 2011
Sub-type Letter to editor, brief commentary or brief communication
DOI 10.1038/mp.2011.95
Open Access Status DOI
Volume 17
Issue 1
Start page 4
End page 7
Total pages 4
Place of publication London, United Kingdom
Publisher Nature Publishing Group
Language eng
Keyword Messenger-Rna
Quality-Control
Mental-Retardation
Nervous-System
Mutations
Transcription
Q-Index Code C1
Q-Index Status Confirmed Code
Grant ID R01 MH081754
Institutional Status UQ
Additional Notes Published online 9 August 2011.

Document type: Journal Article
Sub-type: Letter to editor, brief commentary or brief communication
Collections: Official 2012 Collection
School of Medicine Publications
 
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Citation counts: TR Web of Science Citation Count  Cited 17 times in Thomson Reuters Web of Science Article | Citations
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