Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Deletions in DNAL1 Cause Primary Ciliary Dyskinesia Across North American Indigenous Populations

24 Feb 2023

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cystic Fibrosis Research Advances
Share to Neonatal Respiratory Health Research
Share to Respiratory viral infections research

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 36841509
DOI: 10.1016/j.jpeds.2023.01.023

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Deletions in DNAL1 Cause Primary Ciliary Dyskinesia Across North American Indigenous PopulationsPMID 36841509Read ↗

Primary Ciliary Dyskinesia as a common cause of bronchiectasis in the Canadian Inuit populationSemantic proximity Read ↗

Clinical and genetic analysis of patients with primary ciliary dyskinesia caused by novel DNAAF3 mutationsSemantic proximity Read ↗

The CGG repeat expansion in RILPL1 is associated with oculopharyngodistal myopathy type 4Semantic proximity Read ↗

Unexpected genetic heterogeneity for primary ciliary dyskinesia in the Irish Traveller population.Semantic proximity Read ↗

Mutations in DNAI1 (IC78) cause primary ciliary dyskinesia.Semantic proximity Read ↗

The Genetics of Primary Ciliary Dyskinesia in Puerto RicoSemantic proximity Read ↗

A 3000-year-old founder variant in the DRC1 gene causes primary ciliary dyskinesia in Japan and Korea.Semantic proximity Read ↗

Identification of genetic variants in CFAP221 as a cause of primary ciliary dyskinesiaSemantic proximity Read ↗

Primary ciliary dyskinesia-causing mutations in Amish and Mennonite communities.Semantic proximity Read ↗

Prevalence and founder effect of DRC1 exon 1-4 deletion in Korean patients with primary ciliary dyskinesia.Semantic proximity Read ↗

Population specificity of the DNAI1 gene mutation spectrum in primary ciliary dyskinesia (PCD).Semantic proximity Read ↗

Expansion of GGC Repeat in GIPC1 Is Associated with Oculopharyngodistal MyopathySemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.