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Homozygosity for a missense mutation in the 67 kDa isoform of glutamate decarboxylase in a family with autosomal recessive spastic cerebral palsy: parallels with Stiff-Person Syndrome and other movement disorders

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Description scientific article
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author: Ian M. Carr  Eamonn R Maher  C Geoffrey Woods 

Publication date November 30, 2004
Language English
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http://eprints.whiterose.ac.uk/1057/

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