Gene: MAPT ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4137
Gene Symbol: MAPT
MAPT 		0.040 GeneticVariation disease BEFREE We investigated microglial activation with [(11)C]DAA1106 positron emission tomography (PET), striatal dopaminergic function with l-[beta-(11)C]dopa PET, acetylcholinesterase (AChE) activity with [(11)C]N-methylpiperidin-4-yl acetate PET, and morphologic brain changes with MRI in three persons (aged 38-41 years) with frontotemporal dementia with parkinsonism linked to chromosome 17 (FTDP-17), who were presymptomatic gene carriers (PGCs) from an American kindred with pallidopontonigral degeneration. 20452812 2010
Entrez Id: 4137
Gene Symbol: MAPT
MAPT 		0.040 GeneticVariation disease BEFREE Clinical-pathologic study of biomarkers in FTDP-17 (PPND family with N279K tau mutation). 17196872 2007
Entrez Id: 4137
Gene Symbol: MAPT
MAPT 		0.040 GeneticVariation disease BEFREE Clinical features and disease haplotypes of individuals with the N279K tau gene mutation: a comparison of the pallidopontonigral degeneration kindred and a French family. 12056930 2002
Entrez Id: 4137
Gene Symbol: MAPT
MAPT 		0.040 GeneticVariation disease BEFREE Physiologic assessment of autonomic dysfunction in pallidopontonigral degeneration with N279K mutation in the tau gene on chromosome 17. 12492138 2002