New tool helps uncover rare genetic mutations in common diseases, including Parkinson's (opens in new tab)
Studies of genetics conducted in yeast cells, human neurons, mice or other model systems often reveal networks of genes that could contribute to complex diseases, such as breast cancer, type 2 diabetes and Parkinson's disease. But those findings don't always translate to human biology. Human genetics offers a path to determining which genes among those networks are most relevant to human disease.
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