FTDP-17 with Pick body-like inclusions associated with a novel tau mutation, p.E372G

A novel tau mutation, p.K317N, causes globular glial tauopathy

(2015) Pawel Tacik et al.   ACTA NEUROPATHOLOGICA

A Novel Tau Mutation in Exon 12, p.Q336H, Causes Hereditary Pick Disease

(2015) Pawel Tacik et al.   JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY

Invited review: Frontotemporal dementia caused bymicrotubule-associated protein taugene (MAPT) mutations: a chameleon for neuropathology and neuroimaging

(2015) Bernardino Ghetti et al.   NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY

Invited review: Neuropathology of tauopathies: principles and practice

(2015) G. G. Kovacs   NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY

Ensembl 2015

(2014) Fiona Cunningham et al.   NUCLEIC ACIDS RESEARCH

Novel mutation in MAPT exon 13 (p.N410H) causes corticobasal degeneration

(2013) Naomi Kouri et al.   ACTA NEUROPATHOLOGICA

Tau pathology and neurodegeneration

(2013) Maria Grazia Spillantini et al.   LANCET NEUROLOGY

An integrated map of genetic variation from 1,092 human genomes

(2012)   NATURE

Mutational Analysis in Early-Onset Familial Dementia in the Japanese Population

(2008) Takeshi Ikeuchi et al.   DEMENTIA AND GERIATRIC COGNITIVE DISORDERS

Alzheimer disease-like clinical phenotype in a family with FTDP-17 caused by a MAPT R406W mutation

(2008) S. G. Lindquist et al.   EUROPEAN JOURNAL OF NEUROLOGY

The G389R mutation in theMAPTgene presenting as sporadic corticobasal syndrome

(2008) Giacomina Rossi et al.   MOVEMENT DISORDERS

Frontotemporal dementia and Parkinsonism linked to chromosome 17 in a young Australian patient with the G389R Tau mutation

(2008) N. Bermingham et al.   NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY