Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study
Titel:
Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study
Auteur:
Rosewich, Hendrik Thiele, Holger Ohlenbusch, Andreas Maschke, Ulrike Altmüller, Janine Frommolt, Peter Zirn, Birgit Ebinger, Friedrich Siemes, Hartmut Nürnberg, Peter Brockmann, Knut Gärtner, Jutta