Author Question: The most commonly occurring mutation in people with cystic fibrosis is a deletio (Read 796 times)

Yolanda

  • Hero Member
  • *****
  • Posts: 757
The most commonly occurring mutation in people with cystic fibrosis is a deletion of a single codon. This results in
A) a base-pair substitution.
B) a nucleotide mismatch.
C) a frameshift mutation.
D) a polypeptide missing an amino acid.
E) a nonsense mutation.



coco

  • Hero Member
  • *****
  • Posts: 739

Related Topics

Need homework help now?

Ask unlimited questions for free

Ask a Question

 

Did you know?

Increased intake of vitamin D has been shown to reduce fractures up to 25% in older people.

Did you know?

On average, someone in the United States has a stroke about every 40 seconds. This is about 795,000 people per year.

Did you know?

All adverse reactions are commonly charted in red ink in the patient's record and usually are noted on the front of the chart. Failure to follow correct documentation procedures may result in malpractice lawsuits.

Did you know?

All patients with hyperparathyroidism will develop osteoporosis. The parathyroid glands maintain blood calcium within the normal range. All patients with this disease will continue to lose calcium from their bones every day, and there is no way to prevent the development of osteoporosis as a result.

Did you know?

Vampire bats have a natural anticoagulant in their saliva that permits continuous bleeding after they painlessly open a wound with their incisors. This capillary blood does not cause any significant blood loss to their victims.

For a complete list of videos, visit our video library