Fig. 5From: Typing of hereditary renal amyloidosis presenting with isolated glomerular amyloid deposition(a) The mutation in the APOAI gene of case1, c.220 T > C (red arrow indicates the location of mutant), which resulted in amyloidogenic Trp74Arg variant of ApoA-I. (b) The mutation in the fibrinogen gene of case2, c.1639delA (red arrow indicates the location of mutant), which resulted in an amyloidogenic p. Arg547GlyfsTer21 variant of fibrinogenBack to article page