DOI:
10.1055/s-00000071
Seminars in Neurology
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References
Rosewich H, Thiele H, Ohlenbusch A , et al.
Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study.
Lancet Neurol 2012;
11 (9) 764-773
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