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Biology, 21.07.2019 22:20 yomamafart7
Glut1 is a glucose transporter that is responsible for the facilitated diffusion of glucose across the blood-brain barrier. glut1 deficiency syndrome is a rare genetic disorder where mutations in the gene encoding glut1 reduce or eliminate the function of the glut1 protein. affected individuals suffer from seizures along with a number of potential neurological problems. what would be the most effective therapy to treat patients suffering from this disorder?
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Biology, 22.06.2019 11:30, gymnastcaitlyn1
There are multiple lines of evidence that provide support for common ancestry and evolution. write 3-4 paragraphs describing at least three of them in detail. provide at least one example for each line of evidence.
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