De novo mutations in ATP1A3 cause alternating hemiplegia of childhood - Concepedia

Concepedia

Publication | Open Access

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

DOI Full Paper Access

417

Citations

25

References

2012

Year

Erin L. Heinzen, Kathryn J. Swoboda, Yuki Hitomi, Fiorella Gurrieri, Sophie Nicole, Boukje de Vries, Francesco Danilo Tiziano, Bertrand Fontaine, Sinéad B. Heavin, Eleni Panagiotakaki,

Nature Genetics

Rare DiseasesMendelian DisorderGenetic DisorderGeneticsPathologyMolecular GeneticsAtp1a3 CauseDisease Gene IdentificationMedical GeneticsMedicineNeurogenetics

References

	Year	Citations

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