Brain, Vol. 127, No. 9, 2148,
September 2004
© 2004 Guarantors of Brain
doi: 10.1093/brain/awh299
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:
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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.
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