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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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Literature Corpus work
821fbb27-1251-58a6-a0ea-d1cabd911914
DOI
10.64898/2026.06.17.732907
Open publication

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CFTR function in nasal airway cells from symptomatic and asymptomatic CF heterozygotesDOI 10.64898/2026.06.17.732907
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