Figure 1From: Novel SCARB2 mutation in action myoclonus-renal failure syndrome and evaluation of SCARB2mutations in isolated AMRF features Pedigree of the AMRF family with mutation status. Black symbol: AMRF. Grey symbol: generalized epilepsy and reduction of nerve conduction velocity in the feet. +/+: homozygous mutation, +/-: heterozygous mutation. Symbol #: no information available about genotype status.Back to article page