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.