Condition: FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4


rs1366668789 in TBK1 gene and FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4 PMID 25943890 2015 Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease.

PMID 25803835 2015 Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia.

PMID 25700176 2015 Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways.