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

Clinical and genetic analysis of patients with primary ciliary dyskinesia caused by novel DNAAF3 mutations

12 Jun 2019

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 Genetic and Kidney Cyst Diseases
Share to Pediatric Hepatobiliary Diseases and Treatments

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 31186518
DOI: 10.1038/s10038-019-0609-1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical and genetic analysis of patients with primary ciliary dyskinesia caused by novel DNAAF3 mutationsPMID 31186518Read ↗

Clinical and genetic analysis of two patients with primary ciliary dyskinesia caused by a novel mutation of DNAAF2Semantic proximity Read ↗

Clinical and genetic analysis of two patients with primary ciliary dyskinesia caused by a novel variant of DNAAF2.Semantic proximity Read ↗

The challenge of diagnosing primary ciliary dyskinesia: a commentary on various causative genes and their pathogenic variantsSemantic proximity Read ↗

Novel dynein axonemal assembly factor 1 mutations identified using whole‑exome sequencing in patients with primary ciliary dyskinesia.Semantic proximity Read ↗

Early genetic analysis by next-generation sequencing improves diagnosis of primary ciliary dyskinesia.Semantic proximity Read ↗

Recent advances in primary ciliary dyskinesia geneticsSemantic proximity Read ↗

A novel homozygous mutation in the DNAAF3 gene leads to severe asthenozoospermia and teratospermia.Semantic proximity Read ↗

Clinical manifestations and genotype of primary ciliary dyskinesia diagnosed in Korea: a nationwide, multicenter, retrospective studySemantic proximity Read ↗

Exploring Rare Genetic Mutations in PCD: A Study of 8 Turkish Patients with Novel Gene Alterations Coupled by Their Ciliary Beat Frequency and Confocal Microscopy AnalysesSemantic proximity Read ↗

Clinical and genetic spectrum of primary ciliary dyskinesia in childrenSemantic proximity Read ↗

Primary Ciliary Dyskinesia: Integrating Genetics into Clinical PracticeSemantic proximity Read ↗

Genomic profiling supports the diagnosis of primary ciliary dyskinesia and reveals novel candidate genes and genetic variantsSemantic proximity Read ↗

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