Autosomal dominant movement disorders: molecular analysis of the pathogenesis : linkage analysis of late onset focal dystonia (DYT7), positional cloning of hereditary spastic paraplegia (SPG3), and gene expression studies of spinocerebellar ataxia type 2 (SCA2)
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OCLC: | 787863344 |
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Language: | English |
Published: |
1999.
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Online Resource: | Center for Research Libraries |
Related Items: | Print version:
Autosomal dominant movement disorders: molecular analysis of the pathogenesis. |
Format: | Thesis Monograph Online Resource |