New Findings Explain Genetic Disorder's Unique Shift; Father's Role As Resource Provider Influential In Prader-Willi Syndrome

New findings give insight into the unique characteristics of the birth defect Prader-Willi Syndrome, and at the same time, may help explain how a certain type of gene is expressed in all humans. The research finds that the amount of care a father gives to his child may cause a shift in the syndrome in which its symptoms, in essence, reverse themselves.

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