David McLeod

Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy.

V. Sheffield, M. Batterbury, E. Stone, 2001, Human molecular genetics.

A novel hereditary developmental vitreoretinopathy with multiple ocular abnormalities localizing to a 5-cM region of chromosome 5q13-q14.

W. Wiszniewski, D. McLeod, C. Dodd, 1999, Ophthalmology.