Supplementary Figure

Files in this Data Supplement:

• Supplementary Figure S1 - 1.7 MB (.tif)
  Fundus of six individuals with the 208delG mutation. (a), (b), (c): II:6, IV:4, and III:9, respectively from family A. (d): II:1 from family B. (e) and (f): II:1 and II:2 from family C. Each of the six had heterozygous 208delG mutation in FSCN2. Of the six, three on the left column did not have retinal degeneration. The other three on the right column had LCA (b), CORD (d), or RP (f), respectively. The fundus photo of f (individual II2 of family C) demonstrated pale disc, attenuation of retinal artery, and bone spicule pigmentation although it is of low quality (from old archive file).