Open Access Research article

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

Clare N Lynex*, Ian M Carr, Jack P Leek, Rajgopal Achuthan, Simon Mitchell, Eamonn R Maher, C Geoffrey Woods, David T Bonthon and Alex F Markham

BMC Neurology 2004, 4:20  doi:10.1186/1471-2377-4-20

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