A total of 220 patients with autosomal dominant spastic paraplegia do not display mutations in the SLC33A1 gene (SPG42) - Concepedia

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A total of 220 patients with autosomal dominant spastic paraplegia do not display mutations in the SLC33A1 gene (SPG42)

DOI Full Paper Access

29

Citations

16

References

2010

Year

Nina Schlipf, Christian Beetz, Rebecca Schüle, Giovanni Stévanin, Anne Kjersti Erichsen, Sylvie Forlani, Cécile Zaros, Kathrin N. Karle, Stephan Klebe, Sven Klimpe,

European Journal of Human Genetics

Rare DiseasesGenetic DisorderMedicineGeneticsSlc33a1 GeneProgressive Supranuclear PalsyRehabilitationDisease Gene IdentificationNeuropathologyNeuromuscular Pathology

References

	Year	Citations

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