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A team of researchers from the United States, China, and Taiwan identified three unrelated families with members whose mitochondria contained DNA from both parents. While this discovery could reignite debate about the nature of inheriting mitochondrial DNA, the researchers hope it will open up new ways to treat disease. The story began when a four-year-old patient suffering from fatigue and muscle pain was referred to physician-scientist Taosheng Huang at the Cincinnati Childrens Hospital Medical Center. Others had suggested the boy was showing signs of a mitochondrial disorder, so Huang sequenced and analyzed the boys mitochondrial DNA鈥攁nd found an abnormally high level of heteroplasmy, meaning different mitochondria seemed to contain different genes. Mystified, he sequenced the mitochondrial DNA of the boys other family members, including his sisters, parents, grandparents, and siblings of his parents and grandparents. It appeared that the boy had, as expected, received his strange mitochondria from his mother, who shared the high level of heteroplasmy. But further analysis revealed th [url=https://www.stanley-stanley-cup.us]stanley quencher[/url] at his mother, grandfather, and two of his great aunts had inherited mitochondrial DNA from both parents. Huang reached out to other labs, looking for famili [url=https://www.cups-stanley-cups.us]stanley us[/url] es with members who similarly had high levels of heteroplasmy. He found two with similar patterns, where certain individuals seemed to inherit mitochondrial DNA fro [url=https://www.stanley-cups.us]stanley cup[/url] m both parents, which mothers would then pass on to their own childre