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Long-term course and mutational spectrum of spatacsin-linked spastic paraplegia

Hehr, Ute, Bauer, Peter, Winner, Beate, Bogdahn, Ulrich and Weber, Bernhard H. F. (2007) Long-term course and mutational spectrum of spatacsin-linked spastic paraplegia. Annals of Neurology 27, pp. 381-392.

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OBJECTIVE: Hereditary spastic paraplegias (HSPs) comprise a heterogeneous group of neurodegenerative disorders resulting in progressive spasticity of the lower limbs. One form of autosomal recessive hereditary spastic paraplegia (ARHSP) with thin corpus callosum (TCC) was linked to chromosomal region 15q13-21 (SPG11) and associated with mutations in the spatacsin gene. We assessed the long-term ...


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Item type:Article
Institutions:Medicine > Lehrstuhl für Humangenetik
Identification Number:
18067136PubMed ID
Dewey Decimal Classification:600 Technology > 610 Medical sciences Medicine
Refereed:Yes, this version has been refereed
Created at the University of Regensburg:Yes
Item ID:35225
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