In cystic fibrosis the transport channels for chloride ions do not function properly.This represents a defect in the
A) phospholipids
B) carbohydrates
C) adenosine triphosphate
D) proteins
E) ribonucleic acid

Question

Quizplus · Accepted Answer

The transport channels for chloride ions, also known as the cystic fibrosis transmembrane conductance regulator (CFTR), are proteins that are essential for proper ion transport across cell membranes. In cystic fibrosis, there is a defect in the CFTR protein, which leads to improper chloride ion transport and a range of associated symptoms.

In Cystic Fibrosis the Transport Channels for Chloride Ions Do