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Dominant mutations in ATP1A1, encoding the alpha‐1 isoform of the Na+/K+‐ATPase, have been recently reported to cause an axonal to intermediate type of Charcot‐Marie‐Tooth disease (ie, CMT2DD) and a syndrome with hypomagnesemia, intractable seizures and severe intellectual disability. Here, we describe the first case of hereditary spastic paraplegia (HSP) caused by a novel de novo (p.L337P) variant...
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