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

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

Book ID: 119613085
Publisher: The Lancet
Year: 2012
Tongue: English
Weight: 156 KB
Volume: 11
Category: Article
ISSN: 1474-4465
DOI: 10.1016/s1474-4422(12)70182-5

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