Marfan syndrome is a genetic disorder that affects connective tissue, leading to abnormal skeletal development, lens deformities in the eyes, and heart complications. The disorder is caused by a mutation in the FBN1 gene. The following DNA sequences show a section of the FBN1 gene in an unaffected individual and an individual with Marfan syndrome.
Unaffected individual: CCG-CCG-CTT
Individual with Marfan syndrome: CGG-CCG-CTT
Marfan syndrome is an autosomal dominant disorde
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