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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C. Woods | A. Markham | I. Carr | E. Maher | J. Leek | Clare N Lynex | R. Achuthan | S. Mitchell | David T Bonthon | Bmc Neurology