APA

Lynex C. N., Carr I. M., Leek J. P., Achuthan R., Mitchell S., Maher E. R., Woods C. G., Bonthon D. T. & Markham A. F. (20051212). 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.

Chicago

Lynex Clare N, Carr Ian M, Leek Jack P, Achuthan Rajgopal, Mitchell Simon, Maher Eamonn R, Woods C Geoffrey, Bonthon David T and Markham Alex F. 20051212. 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.

Harvard

Lynex C. N., Carr I. M., Leek J. P., Achuthan R., Mitchell S., Maher E. R., Woods C. G., Bonthon D. T. and Markham A. F. (20051212). 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.

MLA

Lynex Clare N, Carr Ian M, Leek Jack P, Achuthan Rajgopal, Mitchell Simon, Maher Eamonn R, Woods C Geoffrey, Bonthon David T and Markham Alex F. 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. 20051212.