Fig. 3From: Novel in-frame deletion in MFSD8 gene revealed by trio whole exome sequencing in an Iranian affected with neuronal ceroid lipofuscinosis type 7: a case reportPedigree of family affected by neuronal ceroid lipofuscinosis. # de novo or inherited deletion, + heterozygous inferred from pedigree, * heterozygous confirmed by deletion analysis or Sanger sequencing. The arrow shows the proband in the familyBack to article page