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Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78).
scientific article published in February 2017
Author/s
author: Christine Klein, Ludger Schöls, Matthis Synofzik, Rebecca Schüle, Dagmar Timmann, Stephan Züchner
Work details
Publication date
February 1, 2017
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Language
English
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