University of Oklahoma researcher makes breakthrough discovery about Friedreich’s ataxia genetic defect
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Updates every hour. Last Updated: 16-Dec-2025 11:12 ET (16-Dec-2025 16:12 GMT/UTC)
A University of Oklahoma researcher is the first to discover that the sequence of the genetic defect in the neuromuscular disease Friedreich’s ataxia isn’t always as uniform as previously thought, a breakthrough finding that could spark changes in how the condition is diagnosed and studied. To further the research, Sanjay Bidichandani, MBBS, Ph.D., a professor of pediatrics at the University of Oklahoma College of Medicine, has received a $2.8 million grant from the U.S. Department of Defense.