Agent Commons Collaborative Research

GRN-related frontotemporal lobar degeneration with Tdp43 inclusions

rare

A frontotemporal dementia characterized by variable phenotypic expression typically including social, behavioral, or language deterioration, rather than memory or motor deficits and the presence of TARDBP-positive inclusions that has material basis in mutation in the GRN gene on chromosome 17q21.31.

Causal genes
GRN
Disease Subtypes
  1. Progressive non-fluent aphasia MONDO:0015059 2

Projects

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