Fig. 1From: Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial modelDistribution of DNMs in two potential novel autism risk genes (ZNF292, RALGAPB) and CTTNBP2. Dagger symbol indicates the DNMs reported in this study. ZNF292: p.R89* was reported in an ASC patient, p.L943Qfs*5 was reported in an ID patient, p. N1741Lfs*25 was reported in DDD study. RALGAPB: p.M289Vfs*3 was reported in an ASC patient, p.S1287* was reported in an EPI4K patient. CTTNBP2: p.V706Efs*14 was reported in an SSC patientBack to article page