Fig. 2From: Genotype-phenotype analysis of von Hippel-Lindau syndrome in Korean families: HIF-α binding site missense mutations elevate age-specific risk for CNS hemangioblastomaDistribution of germline mutations in VHL patients. Three exons are shown by boxes and α/β domains are indicated by colored boxes. The horizontal bars indicate binding domains. A splice site mutation, c.464-1G > T is not shown in this figureBack to article page