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Biology, 24.06.2021 19:30, lucahoffmannm
The mutation in the FBN1 gene that causes Marfan syndrome influences the phenotypic outcomes of several traits in the human body (elongated head, limbs, and digits; lung and eye problems; and heart valve and vessel defects). In your current research you identify a second gene, called FCD3, whose expression is affected by the FBN1 mutation. This scenario of genes interacting with each other to determine phenotype is an example of .
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