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Comment

. 2012 Sep;11(9):741-3.

doi: 10.1016/S1474-4422(12)70185-0. Epub 2012 Aug 2.

Clinical spectrum of disease associated with ATP1A3 mutations

Laurie J Ozelius¹

Affiliations

Affiliation

¹ Department of Genetics and Genomic Sciences and Department of Neurology, Mount Sinai School of Medicine, 1 Gustave L Levy Place, New York, NY 10029, USA. laurie.ozelius@mssm.edu

PMID: 22857851
DOI: 10.1016/S1474-4422(12)70185-0

Comment

Clinical spectrum of disease associated with ATP1A3 mutations

Laurie J Ozelius. Lancet Neurol. 2012 Sep.

. 2012 Sep;11(9):741-3.

doi: 10.1016/S1474-4422(12)70185-0. Epub 2012 Aug 2.

Author

Laurie J Ozelius¹

Affiliation

¹ Department of Genetics and Genomic Sciences and Department of Neurology, Mount Sinai School of Medicine, 1 Gustave L Levy Place, New York, NY 10029, USA. laurie.ozelius@mssm.edu

PMID: 22857851
DOI: 10.1016/S1474-4422(12)70185-0

No abstract available

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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

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