pLenti HsATP13A2 D508N Citations (1)
Originally described in: ATP13A2 deficiency disrupts lysosomal polyamine export.van Veen S, Martin S, Van den Haute C, Benoy V, Lyons J, Vanhoutte R, Kahler JP, Decuypere JP, Gelders G, Lambie E, Zielich J, Swinnen JV, Annaert W, Agostinis P, Ghesquiere B, Verhelst S, Baekelandt V, Eggermont J, Vangheluwe P Nature. 2020 Feb;578(7795):419-424. doi: 10.1038/s41586-020-1968-7. Epub 2020 Jan 29. PubMed Journal
Articles Citing pLenti HsATP13A2 D508N
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Kufor-Rakeb syndrome-associated psychosis: a novel loss-of-function ATP13A2 variant and response to antipsychotic therapy.
Colijn MA, Vrijsen S, Au PYB, Abou El Asrar R, Houdou M, Van den Haute C, Sarna J, Montgomery G, Vangheluwe P.
Neurogenetics. 2024 Jul 18. doi: 10.1007/s10048-024-00767-7.
PubMed
Associated Plasmids |
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