[The current results imply further genetic heterogeneity of frontotemporal dementia, as we detected only one GRN-linked family (about 1%)/value of discovering large kindred includes the possibility of a longitudinal study of GRN mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
Gene-disease associations inferred from text-mining the literature.
DisGeNET evidence - LITERATURE