Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients
Fig 2
ALZ-6 family pedigree and sequencing chromatograms.
(A) The arrow indicates the proband. Black filled symbols: affected patients; white symbols: unaffected family members. N: Normal, M: the c.708+6_9delTGAG deletion. CVA: cerebral vascular accident, AO: age at disease onset, AD: age of death. (B) Sequencing chromatograms show the presence of GRN c.708+6_9delTGAG deletion in the index patient III-3 that is not seen in individuals III-1 and III-4.