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Spinal Muscular Atrophy: Indians who need $2 1m drug to fight a rare disease
Most people with rare genetic diseases are unable to access life-saving medicines due to high costs.
New york
United states
Tamil nadu
United kingdom
Zeba gufran
Chandrakant lahariya
Sheffali gulati
Cherylann mollan
Kalpana sharma
India institute of medical sciences
Drug administration
New york times
National health service
Spinal muscular atrophy
Duchenne muscular dystrophy
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