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Examination of an Estonian patient helped discover a new form of muscular dystrophy
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Examination of an Estonian patient helped discover a new form of muscular dystrophy

ESTONIAN RESEARCH COUNCIL IMAGE: PROFESSOR OF CLINICAL GENETICS OF THE UNIVERSITY OF TARTU KATRIN ÕUNAP. CREDIT: UNIVERSITY OF TARTU In about a quarter of patients with hereditary diseases, the cause of the disease remains unclear even after extensive genetic testing. One reason is that we still do not know enough about the function of many genes. Of...