We are very supportive. The European Organisation for Rare Disorders, the National Organization for Rare Disorders in the U.S., and the Canadian Organization for Rare Disorders have actually signed a joint memorandum of understanding to say that we support international registries, and as David says, they need to have common elements.
The other thing I will mention is that the NIH, the National Institutes of Health in the U.S., has just in fact helped to launch a large genetic registries website called Registries for All. It's meant to be exactly for this purpose, to provide a common platform on which you can have individual genetic diseases registered. Patient access is available. We're very much encouraging all countries to go to a common platform so that the data may in fact be shared. Patient privacy can be protected. As David said, we're very supportive of it, and we're also very proud that Canada quite frankly is again one of the leading partners in helping to move this kind of an initiative forward.