Extended investigation of tau and mutation screening of other candidate genes on chromosome 17q21 in a Swedish FTDP-17 family
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference41 articles.
1. Structure and novel exons of the human .tau. gene
2. Clinical Characteristics of a Chromosome 17--Linked Rapidly Progressive Familial Frontotemporal Dementia
3. Interaction of tau with the neural plasma membrane mediated by tau's amino-terminal projection domain.
4. Familial non-specific dementia maps to chromosome 3
5. Comparative Biochemistry of Tau in Progressive Supranuclear Palsy, Corticobasal Degeneration, FTDP-17 and Pick's Disease
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