HUM-MOLGEN DIAGnostics/Clinical Research


nephrotic syndrome/WT1 gene

We are investigating the molecular basis of congenital nephrotic syndrome. Specifically, we are testing the possibility that mutations of the Wilms tumor (WT1) gene are responsible for at least a subset of diffuse mesangial sclerosis. Ethical approval has been obtained for this project.We require DNA, blood, or post-mortem tissue from patients with DMS.

Many thanks

Dr. Ania Koziell

If you can help please contact me at the above email address
or by FAX 44-171-916-0011, or by 'phone 44-171-242-9789 x 2635
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