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Figure 3 | BMC Neurology

Figure 3

From: 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

Figure 3

Electropherograms of the sequence of the exon 1 SNP of GAD1 identified in the process of mutational analysis. (A) and (B) show the normal C variant in the forward and reverse directions, respectively. (C) and (D) show the alternative G variant in the forward and reverse directions, respectively. This variant was only found in affected individuals of family B. No heterozygous individuals were identified for this nucleotide variant.

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BMC Neurology

ISSN: 1471-2377

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