Since it was identified through genetic testing in the early 2000s, ataxia with oculomotor apraxia type 2 (AOA2) has become the second most commonly diagnosed form of recessive ataxia. But while more individuals are being diagnosed with AOA2, research on the disease remains scant. That paucity in data shouldn't last long, however, thanks to a team of researchers at the University of Minnesota's world-renowned Center for Magnetic Resonance Research (CMRR).
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