The novel Tau mutation G335S: clinical, neuropathological and molecular characterization
The novel Tau mutation G335S: clinical, neuropathological and molecular characterization
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Germany: Springer Nature B.V
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Language
English
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Publisher
Germany: Springer Nature B.V
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Mutations in Tau cause the inherited neurodegenerative disease, frontotemporal dementia and Parkinsonism linked to chromosome 17 (FTDP-17). Known coding region mutations cluster in the microtubule-binding region, where they alter the ability of tau to promote microtubule assembly. Depending on the tau isoforms, this region consists of three or four...
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Full title
The novel Tau mutation G335S: clinical, neuropathological and molecular characterization
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TN_cdi_proquest_miscellaneous_70263127
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_70263127
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ISSN
0001-6322
E-ISSN
1432-0533
DOI
10.1007/s00401-006-0182-5
