This site needs JavaScript to work properly. Please enable it to take advantage of the complete set of features!

Skip to main page content

Add to Collections

Your saved search

Name of saved search:

Search terms:

Test search terms

Would you like email updates of new search results?

Yes
No

Email: (change)

Frequency:

Which day?

Which day?

Report format:

Send at most:

Send even when there aren't any new results

Optional text in email:

Your RSS Feed

Comment

. 2013 Jan;83(1):32-3.

doi: 10.1111/cge.12031. Epub 2012 Oct 29.

Mutations in ATP1A3 cause alternating hemiplegia of childhood

F Aminkeng¹

Affiliations

Affiliation

¹ The Canadian Pharmacogenomic Network for Drug Safety, Center for Molecular Medicine and Therapeutics, Department of Medical Genetics, University of British Columbia, Vancouver, Canada. folefac@cmmt.ubc.ca

PMID: 23043298
DOI: 10.1111/cge.12031

Comment

Mutations in ATP1A3 cause alternating hemiplegia of childhood

F Aminkeng. Clin Genet. 2013 Jan.

. 2013 Jan;83(1):32-3.

doi: 10.1111/cge.12031. Epub 2012 Oct 29.

Author

F Aminkeng¹

Affiliation

¹ The Canadian Pharmacogenomic Network for Drug Safety, Center for Molecular Medicine and Therapeutics, Department of Medical Genetics, University of British Columbia, Vancouver, Canada. folefac@cmmt.ubc.ca

PMID: 23043298
DOI: 10.1111/cge.12031

No abstract available

PubMed Disclaimer

Comment on

Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study.
Rosewich H, Thiele H, Ohlenbusch A, Maschke U, Altmüller J, Frommolt P, Zirn B, Ebinger F, Siemes H, Nürnberg P, Brockmann K, Gärtner J. Rosewich H, et al. Lancet Neurol. 2012 Sep;11(9):764-73. doi: 10.1016/S1474-4422(12)70182-5. Epub 2012 Jul 30. Lancet Neurol. 2012. PMID: 22850527

Publication types

Actions

LinkOut - more resources

Full Text Sources
- Ovid Technologies, Inc.
- Wiley
Other Literature Sources
- scite Smart Citations