Fig. 1From: A novel RAB39B mutation and concurrent de novo NF1 mutation in a boy with neurofibromatosis type 1, intellectual disability, and autism: a case reportPedigree and clinical features of proband with concurrent RAB39B and NF1 mutations. An asterisk designates subjects recruited for the genetic study; an arrow indicates proband. Sequence data for mutant alleles and their family segregation are shown below the symbolBack to article page