Article
CFTR function in nasal airway cells from symptomatic and asymptomatic CF heterozygotes
2026-06-18
Abstract excerpt
<h4>Structured Abstract</h4> <h4>Rationale</h4> An estimated 25 million people worldwide have one deleterious variant in the cystic fibrosis transmembrane conductance regulator ( CFTR ) gene. Chronic respiratory disease symptoms are at an increased prevalence in cystic fibrosis (CF) heterozygotes. <h4>Objectives</h4> Determine the level of CFTR function in CF heterozygotes compared to individuals without CF-c...
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Identifiers and source
- Literature Corpus work
- 821fbb27-1251-58a6-a0ea-d1cabd911914
- DOI
- 10.64898/2026.06.17.732907
