CAG repeat disorder models and human neuropathology: similarities and differences
CAG repeat disorder models and human neuropathology: similarities and differences
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Publisher
Berlin/Heidelberg: Springer-Verlag
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Language
English
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Publisher
Berlin/Heidelberg: Springer-Verlag
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Scope and Contents
Contents
CAG repeat diseases are hereditary neurodegenerative disorders caused by expansion of a polyglutamine tract in each respective disease protein. They include at least nine disorders, including Huntington’s disease (HD), dentatorubral pallidoluysian atrophy (DRPLA), spinal and bulbar muscular atrophy (SBMA), and the spinocerebellar ataxias SCA1, SCA2...
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Full title
CAG repeat disorder models and human neuropathology: similarities and differences
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TN_cdi_proquest_journals_211859950
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_211859950
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ISSN
0001-6322
E-ISSN
1432-0533
DOI
10.1007/s00401-007-0287-5
