Novel haplotypes in 17q21 are associated with progressive supranuclear palsy-Reference-Cited by-同舟云学术

Novel haplotypes in 17q21 are associated with progressive supranuclear palsy

Published:2004 Issue:2 Volume:56 Page:249-258
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Pastor Pau,Ezquerra Mario,Perez J. Christian,Chakraverty Sumi,Norton Joanne,Racette Brad A.,McKeel Dan,Perlmutter Joel S.,Tolosa Eduardo,Goate Alison M.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference27 articles.

1. Segregation of a Missense Mutation in the Microtubule-Associated Protein Tau Gene with Familial Frontotemporal Dementia and Parkinsonism

2. Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17

3. Mutation in the tau gene in familial multiple system tauopathy with presenile dementia

4. Familial atypical progressive supranuclear palsy associated with homozigosity for the delN296 mutation in the tau gene

5. New developments in frontotemporal dementia and parkinsonism linked to chromosome 17

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