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Comment
. 2017 Dec 1;140(12):e74.
doi: 10.1093/brain/awx282.

Reply: Complicated hereditary spastic paraplegia due to ATP13A2 mutations: what's in a name?

Rebecca Schüle  1   2
Affiliations
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Reply: Complicated hereditary spastic paraplegia due to ATP13A2 mutations: what's in a name?

Rebecca Schüle. Brain. .
No abstract available

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References

    1. de Bot S, Kamsteeg E-J, van de Warrenburg BPC. Complicated hereditary spastic paraplegia due to ATP13A2 mutations: what’s in a name? Brain 2017; 140: e73. - PubMed
    1. Bras J, Verloes A, Schneider SA, Mole SE, Guerreiro RJ. Mutation of the parkinsonism gene ATP13A2 causes neuronal ceroid-lipofuscinosis. Hum Mol Genet 2012; 21: 2646–50. - PMC - PubMed
    1. Estrada-Cuzcano A, Martin S, Chamova T, Synofzik M, Timmann D, Holemans T, et al. Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78). Brain 2017; 140(Pt 2): 287–305. - PMC - PubMed
    1. Kara E, Tucci A, Manzoni C, Lynch DS, Elpidorou M, Bettencourt C, et al. Genetic and phenotypic characterization of complex hereditary spastic paraplegia. Brain 2016; 139(Pt 7): 1904–18. - PMC - PubMed
    1. Marras C, Lang A, van de Warrenburg BP, Sue CM, Tabrizi SJ, Bertram L, et al. Nomenclature of genetic movement disorders: recommendations of the international Parkinson and movement disorder society task force. Mov Disord 2016; 31: 436–57. - PubMed

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