David Harrison

WT1 is a key regulator of podocyte function: reduced expression levels cause crescentic glomerulonephritis and mesangial sclerosis.

A. Schedl, A. Clarke, M. Gubler, 2002, Human molecular genetics.

Spondyloepiphyseal dysplasia and precocious osteoarthritis in a family with an Arg75→Cys mutation in the procollagen type II gene (COL2A1)

S. Jimenez, D. Prockop, R. Knowlton, 1993, Human Genetics.

A zinc finger truncation of murine WT1 results in the characteristic urogenital abnormalities of Denys-Drash syndrome.

A. Brookes, D. Porteous, K. Miyagawa, 1999, Proceedings of the National Academy of Sciences of the United States of America.