Conflict of interest: None
A novel ALDH5A1 mutation is associated with succinic semialdehyde dehydrogenase deficiency and severe intellectual disability in an Iranian family
Article first published online: 4 JUL 2013
Copyright © 2013 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part A
Volume 161, Issue 8, pages 1915–1922, August 2013
How to Cite
2013. A novel ALDH5A1 mutation is associated with succinic semialdehyde dehydrogenase deficiency and severe intellectual disability in an Iranian family. Am J Med Genet Part A. 161A:1915–1922., , , , , , , , , , , .
- Issue published online: 24 JUL 2013
- Article first published online: 4 JUL 2013
- Manuscript Accepted: 15 APR 2013
- Manuscript Received: 18 JUL 2012
- Iranian National Science Foundation and the Max Planck Innovation Fund
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