The tau gene in progressive supranuclear palsy: exclusion of mutations in coding exons and exon 10 splice sites, and identification of a new intronic variant of the disease-associated H1 haplotype in Italian cases. [electronic resource]

By: Contributor(s): Producer: 20000204Description: 61-5 p. digitalISSN:
  • 0304-3940
Subject(s): Online resources: In: Neuroscience letters vol. 274
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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