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)

Rudnicki, Dobrila Doda

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RWTH Aachen University

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)

dc:creator Rudnicki, Dobrila Doda

dc:date1999

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Author dc:creator: Rudnicki, Dobrila Doda
Contributors dc:contributor: Auburger, Georg

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Statement dc:rights: info:eu-repo/semantics/closedAccess
Language dc:language: eng

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Identifier: https://publications.rwth-aachen.de/search?p=id:%22RWTH-CONV-118221%22
OAI record oai:identifier: https://publications.rwth-aachen.de/oai2d?verb=GetRecord&metadataPrefix=oai_dc&identifier=oai%3Apublications.rwth-aachen.de%3A56096

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aachen
1999

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Rudnicki, Dobrila Doda. 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). 1999. https://publications.rwth-aachen.de/record/56096

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)

Author and committee

Rights

Identifiers

Chain of custody

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