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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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Figure

Table 1: Oligonucleotide primer used in the amplification of GAD1 exons.
Table 2: Approximate sizes of YAC clones spanning the 2q24-31.1 autosomal recessive spastic CP disease gene locus, used to estimate
Figure 2Annotation of two pedigrees of spastic autosomal recessive CP families and corresponding linkage mapping data
Table 4: GAD1 single nucleotide substitutions detected on mutation analysis and occurring in sequences submitted to NCBI SNP database and in the literature
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