Figure 1
From: The causal mutation in ARR3 gene for high myopia and progressive color vision defect
Pedigree of the family affected by X-linked dominant high myopia and defective color vision. Only IV-10 had late-onset high myopia, arising in his middle school years, other high myopia patients were all early-onset high myopia (eoHM). Gray color: protan/deutan color vision defect; black color: high myopia. ?: uncertain manifestation. +: available family members.
