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Fahed, A. et al. (n.d.). UBQLN2 mutation causing heterogeneous X‐linked dominant neurodegeneration. Annals of neurology. 75 (5), pp. 793-798. [Online].
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Fahed, A. et al. (n.d.). UBQLN2 mutation causing heterogeneous X‐linked dominant neurodegeneration. Annals of neurology. 75 (5), pp. 793-798. [Online].