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A novel locus for autosomal dominant « uncomplicated » hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3..
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A de novo SPAST mutation leading to somatic mosaicism is associated with a later age at onset in HSP..
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A new locus for autosomal recessive spastic paraplegia (SPG32) on chromosome 14q12-q21..
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