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Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study

Author:

Hendrik Rosewich,Holger Thiele,Andreas Ohlenbusch,Ulrike Maschke,Janine Altmüller,Peter Frommolt,Birgit Zirn,Friedrich Ebinger,Hartmut Siemes,Peter Nürnberg,Knut Brockmann,Jutta Gärtner

Publication:

The Lancet Neurology

Publisher:

Elsevier

Date:

September 2012

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