Questionnaire-assessed genotypes and associations with symptoms in primary ciliary dyskinesia.

Collecting genetic information by questionnaire from people with PCD is feasible. This study confirmed typical differences in laterality defects and age at diagnosis between genotypes but found that symptoms were equally common across genotypes. https://bit.ly/4bvKW4R.

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Publication Details

Journal
Open Access CRIS of the University of Bern
Published
2024-09-01
DOI
https://doi.org/10.48620/76988
Primary Topic
Cystic Fibrosis Research Advances
Type
article
Field-Weighted Citation Impact
0.00
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article

Questionnaire-assessed genotypes and associations with symptoms in primary ciliary dyskinesia.

Open Access CRIS of the University of Bern
Cystic Fibrosis Research Advances
article

Questionnaire-assessed genotypes and associations with symptoms in primary ciliary dyskinesia.

article en

Abstract

Collecting genetic information by questionnaire from people with PCD is feasible. This study confirmed typical differences in laterality defects and age at diagnosis between genotypes but found that symptoms were equally common across genotypes. https://bit.ly/4bvKW4R.

Open Access CRIS of the University of Bern
Bremer Umweltinstitut (DE), Clinical Research Management (US)
Openalex Percentile: Top 51%
Cystic Fibrosis Research Advances
DOIOpen Access PDFOpenAlex
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Questionnaire-assessed genotypes and associations with symptoms in primary ciliary dyskinesia. · Open Access CRIS of the University of Bern (2024) | TGRS Research Map | TGRS