This article refers to:
Thiagalingam S, McGee TL, Weleber RG, Sandberg MA, Trzupek KM, Berson EL, Dryja TP. Novel Mutations in the KCNV2 Gene in Patients with Cone Dystrophy and a Supernormal Rod Electroretinogram. Ophthalmic Genet. 2007;28:135–142.
The authors of this article would like to notify the Ophthalmic Genetics readers of an error in Table 3, the last line of the middle column should read: c.778T/c.866delC (not c.778T/c.867delC). This was also referred to in text, on page 137 left column, second paragraph.