Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study (Q50792593)
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scientific article published on 30 July 2012
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study |
scientific article published on 30 July 2012 |
Statements
Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study (English)
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Peter Nürnberg
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Janine Altmüller
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Holger Thiele
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Hendrik Rosewich
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Andreas Ohlenbusch
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Ulrike Maschke
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Birgit Zirn
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Friedrich Ebinger
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Hartmut Siemes
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Knut Brockmann
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Jutta Gärtner
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30 July 2012
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11
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9
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764-773
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