rs63751273, MAPT

N. diseases: 42
Disease: Language Disorders ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Language Disorders
CUI: C0023015
Disease: Language Disorders
0.010 GeneticVariation BEFREE We found reduced mRNA and protein expression of FOXP2 in frontal cortex area 8 in Pick's disease, and frontotemporal lobar degeneration-tau linked to P301L mutation presenting with language impairment in comparison with age-matched controls and cases with parkinsonian variant progressive supranuclear palsy. 27497476 2016