Neuropathology of classic myotonic dystrophy type 1 is characterized by both early initiation of pri...
Neuropathology of classic myotonic dystrophy type 1 is characterized by both early initiation of primary age-related tauopathy of the hippocampus and unique 3-repeat tauopathy of the brainstem
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Oxford University Press
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English
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Oxford University Press
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Myotonic dystrophy type 1 (DM1) is an inherited autosomal-dominant condition that induces altered splicing of transcripts, including MAPT, leading to a distinctive abnormal deposition of tau protein in the CNS. We characterized the tau isoforms of abnormal depositions in the brains of 4 patients with classic DM1 by immunohistochemistry using isofor...
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Full title
Neuropathology of classic myotonic dystrophy type 1 is characterized by both early initiation of primary age-related tauopathy of the hippocampus and unique 3-repeat tauopathy of the brainstem
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TN_cdi_gale_infotracmisc_A768425139
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_gale_infotracmisc_A768425139
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ISSN
0022-3069
DOI
10.1093/jnen/nlac097
