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