August F. Deutman

Clinical characterization, linkage analysis, and PRPC8 mutation analysis of a family with autosomal dominant retinitis pigmentosa type 13 (RP13)

A. Deutman, F. Cremers, C. Hoyng, 2002, Ophthalmic genetics.

Autosomal dominant central areolar choroidal dystrophy caused by a mutation in codon 142 in the peripherin/RDS gene.

A. Deutman, P. Heutink, B. Oostra, 1996, American journal of ophthalmology.