Identification of a novel mutation in ATP13A2 associated with a complicated form of hereditary spastic paraplegia.
Yasuko OdakeKishin KohYoshihisa TakiyamaHiroyuki IshiuraShoji TsujiMasahito YamadaMitsuhiro YoshitaPublished in: Neurology. Genetics (2020)
Our study further broadens the clinical spectrum associated with ATP13A2 mutations.
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