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Lynex, C.N., Carr, I.M., Leek, J.P. et al. (6 more authors) (2004) 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. BMC Neurology, 4 (20). ISSN 1471-2377

This list was generated on Sun Nov 17 12:58:40 2019 GMT.