Clinical features of hereditary spastic paraplegia due to spastin mutation
Neurology McDermott et al.
67: 45
Data Supplement
Two tables; two Word documents.
Files in this Data Supplement:
E1
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Table (E)T.1 - All 17 exons of the SPG4 gene were amplified from genomic DNA using these primers which have universal M13 tags (underlined) attached; Word document.
E2
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Table (E)T.2 - Polymorphisms identified in spastin; Word document.
