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MAPT p.V363I mutation: A rare cause of corticobasal degeneration. (2019)

First Author: Ahmed S

Attributed to: Investigation of the genetic and functional determinants of disease progression in Progressive Supranuclear Palsy funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1212/nxg.0000000000000347

PubMed Identifier: 31404212

Publication URI: http://europepmc.org/abstract/MED/31404212

Type: Journal Article/Review

Volume: 5

Parent Publication: Neurology. Genetics

Issue: 4

ISSN: 2376-7839