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Can GWAS identify the causes of variable expression and progression in Charcot-Marie-Tooth disease?
Charcot-Marie-Tooth disease (CMT) is one of the most common inherited neurological disorders, affecting approximately 1 in 2,500 people in the United States. Since 1991, 90 different genes causing CMT subtypes have been identified, but the severity of the disease can vary even among families with the same genetic variant. Disease-modifying genes, epigenetics, mitochondrial involvement, exercise levels, diet, and environmental...
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