Associated Papers
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.
Lynex CN et al.
Bmc Neurology, 2004
The association between GAD1 gene polymorphisms and cerebral palsy in Chinese infants.
Lin S et al.
Tsitologiia I Genetika, 0
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