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"For me - I am simply pleased that I left what I entered with - a level of sight that gives me my freedom. What more could I ask for?" Professor Ali said that the team now hoped to treat children: "The next stage is to increase the dose of the gene which we anticipate will improve the outcome - and it's also to treat younger patients, who have better residual vision and in whom we expect to see a much greater benefit." Although the genetic condition that is being treated is rare, the researchers believe that their technique could be used to treat a wide variety of sight disorders, possibly even age-related sight loss. Mr Bainbridge added: "This is only the beginning. "What we've demonstrated so far is proof of principle that gene therapy can be used to treat a particular gene disorder." The research, which has been funded by the Department of Health, has been published online in the New England Journal of Medicine. Health Minister Dawn Primarolo said: "This is absolutely brilliant. "It's been done here in the UK with the expertise of the NHS and the science and research of the Department of Health all coming together to offer such hope for gene therapy for the correction of sight - but also for gene therapy generally." David Head, of the British Retinitis Pigmentosa Society, thanked Professor Ali and his team for their "outstanding" work. He said: "Of course, we must temper our excitement and enthusiasm with an acknowledgement that these are very early days, and the trial is working on one flawed gene."
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