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Table 1 Clinical features and serum amino acid levels of the patients in the present family and those in the earlier reported families

From: SPG9A with the new occurrence of an ALDH18A1 mutation in a CMT1A family with PMP22 duplication: case report

  1. HSP hereditary spastic paraplegia, CMT Charcot-Marie-Tooth disease, NA not available, F female, M male, →: normal, ↑: increased, ↓: decreased