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 		0.120 GeneticVariation disease BEFREE A new MAPT deletion in a case of speech apraxia leading to corticobasal syndrome. 29969053 2018
Entrez Id: 4137
Gene Symbol: MAPT
MAPT 		0.120 GeneticVariation disease BEFREE A Novel MAPT Mutation Causing Corticobasal Syndrome Led by Progressive Apraxia of Speech. 26402116 2015
Entrez Id: 4137
Gene Symbol: MAPT
MAPT 		0.120 Biomarker disease HPO