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For Anderson family, an early bet on SMA gene therapy

When Malachi Anderson was diagnosed with a rare and often deadly disease called spinal muscular atrophy (SMA) as an infant nearly four years ago, his parents Tina and Torence had a decision to make.

Original source: http://feeds.reuters.com/~r/reuters/INhealth/~3/kedI42PVkYk/for-anderson-family-an-early-bet-on-sma-gene-therapy-idINKCN1SU2FC

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