A clinical, genetic and biochemical study of SPG7 mutations in hereditary spastic paraplegia

The authors wish to apologise for the following error which occurred in Table 3 of the above paper: SPG7 mutations detected AMINO ACID ABBREVIATIONS: A = alanine, E = glutamic acid, F = phenylalanine, G = glycine, L = leucine, R = arginine, S = serine, V = valine SPG7 mutations detected AMINO ACID ABBREVIATIONS: A = alanine, E = glutamic acid, F = phenylalanine, G = glycine, L = leucine, R = arginine, S = serine, V = valine Patient 1, exon1, mutation is 28G→T not 28G→A as published. The amino acid change remains the same A10S. The corrected table is below.