Fig. 5From: Hereditary cardiac amyloidosis associated with Pro24Ser transthyretin mutation: a case reporta DNA sequencing of transthyretin indicates mutation in exon2 with a nucleotide substitution at 70th (C70T), resulting in Pro24Ser variant of the transthyretin protein. b Genotyping of transthyretin in family members of the patient. Arrow indicates the proband. Individuals with heterozygous Pro24Ser mutation (filled symbols); wild-type (shaded); not tested (open)Back to article page