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

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

DOI Full Paper Access

263

Citations

37

References

2012

Year

Hendrik Rosewich, Hölger Thiele, Andreas Ohlenbusch, Ulrike Maschke, Janine Altmüller, Peter Frommolt, Birgit Zirn, Friedrich Ebinger, H. Siemes, Peter Nürnberg,

The Lancet Neurology

Heterozygous De-novo MutationsMendelian DisorderGenetic DisorderGeneticsPathologyMolecular GeneticsDisease Gene IdentificationGenomicsMedicineVariant Interpretation

References

	Year	Citations

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