For Anderson family, an early bet on SMA gene therapy https://reut.rs/2M7GfI2 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. http://bit.ly/hzQbMP May 25, 2019 at 12:57AM

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.

from Reuters: Top News https://reut.rs/2M7GfI2