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						 Gene 
						therapy breakthrough wins world's largest vision award 
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		[September 05, 2018]  
		LISBON (Reuters) - Seven scientists in the 
		United States and Britain who have come up with a revolutionary gene 
		therapy cure for a rare genetic form of childhood blindness won a 1 
		million euro ($1.15 million)prize on Tuesday, Portugal's Champalimaud 
		Foundation said. | 
        
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			 Established in 2006, the annual award for work related to vision is 
			one of the world's largest science prizes, more than the latest 9 
			million Swedish crown ($987,000) Nobel Prize in Physiology or 
			Medicine. 
 "This is the first, and still only example of successful gene 
			therapy in humans that corrects an inherited genetic defect and is 
			therefore a milestone in medical therapeutics," said Alfred Sommer, 
			Dean Emeritus of the Johns Hopkins Bloomberg School of Public Health 
			and chairman of the award jury.
 
 One of those honored, Michael Redmond of the National Eye Institute 
			in Maryland, had traced the cause of the disease, Leber congenital 
			amaurosis (LCA), to a mutated gene.
 
			
			 
			Three cooperating research teams later managed to replace the gene 
			in the eye, restoring vision to treated children and adults with one 
			form of LCA and "enabling the entire field of gene therapy for human 
			disease", the foundation said. 
			
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			These teams are comprised of U.S. scientists Jean Bennett and Albert 
			Maguire; Samuel Jacobson and William Hauswirth; and Britons Robin 
			Ali and James Bainbridge.
 Their gene augmentation therapy involved the delivery of healthy 
			genes using engineered harmless viruses, described by the foundation 
			as "an elegant solution".
 
 The foundation, which focuses on neuroscience and oncology research 
			at its Lisbon base, was set up at the bequest of Portugal's late 
			industrialist Antonio Champalimaud who died in 2004. The first 
			vision prize was awarded in 2006.
 
 (Reporting by Andrei Khalip; Editing by Alison Williams)
 
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