Homozygosity for a missense mutation in the 67 kDa isoform...

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

Clare N Lynex, Ian M Carr, Jack P Leek, Rajgopal Achuthan, Simon Mitchell, Eamonn R Maher, C Geoffrey Woods, David T Bonthon, Alex F Markham
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Volume:
4
Language:
english
DOI:
10.1186/1471-2377-4-20
Date:
December, 2004
File:
PDF, 553 KB
english, 2004
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