An individual heterozygous for cystic fibrosis ________
A) cannot have children with cystic fibrosis
B) is a carrier
C) will have children who are all carriers of cystic fibrosis
D) has cystic fibrosis
B
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Cystic fibrosis is most often caused by the CFTR?F508 mutation. This mutation:
A. reduces the function of a chloride ion channel. B. increases ATP binding to chloride. C. is autosomal dominant. D. causes symptoms in carriers.
Of the following proteins, which would be a good target for drug therapy if one needed to interfere with breaking down the microfilament network?
A) profilin B) CapZ C) gelsolin D) tropomodulin E) calmodulin
what membrane disrupting exotoxin secreted by Staph aureus cause leukocyte lyses?
What will be an ideal response?
two main stages of digestion
What will be an ideal response?