CAPN1 mutations: Expanding the CAPN1-related phenotype: From hereditary spastic paraparesis to spastic ataxia

Shetty, Aakash; Gan-Or, Ziv; Ashtiani, Setareh; Ruskey, Jennifer A.; Warrenburg, B.P.C. van de; Wassenberg, T.; Kamsteeg, E.J.; Rouleau, G.A.; Suchowersky, Oksana

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Publication year

2019

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Warrenburg, B.P.C. van de

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European Journal of Medical Genetics, 62, 12, (2019), article UNSP 103605

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1769-7212

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https://doi.orghttps://doi.org/10.1016/j.ejmg.2018.12.010

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Article / Letter to editor

Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/212346

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CAPN1 mutations: Expanding the CAPN1-related phenotype: From hereditary spastic paraparesis to spastic ataxia

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