People with sickle-cell disease have _______ abnormality.
A) a phenylalanine hydrolyase
B) an oncogene
C) a cholesterol transport
D) a hemoglobin
E) None of the above
Correct Answer:
Verified
Q9: Most genetic diseases are rare because
A) each
Q10: Genetic diagnosis by DNA testing
A) detects only
Q11: In fragile-X syndrome,
A) females are affected more
Q12: In sickle-cell disease, one amino acid is
Q13: Which of the following is not a
Q15: Mutations are
A) heritable changes in the sequence
Q16: An example of a gain of function
Q17: Current treatments for genetic diseases include all
Q18: Silent mutations have no effect on amino
Q51: Multifactorial (complex) diseases
A) are less common than
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