AAVLife series A: $12M for Friedreich's ataxia gene therapy program
By Randy Osborne
Tuesday, April 15, 2014
About 13 years ago, when Amber Salzman's son and two nephews were diagnosed with adrenoleukodystrophy (ALD), a genetic brain disorder, she didn't know much about rare diseases at all. That's changed for the CEO of Paris-based AAVLife, which with $12 million in series A money is taking aim at another: Friedreich's ataxia (FA).
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