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Article

Mutations in DNAI1 (IC78) cause primary ciliary dyskinesia.

Chest - 1 Mar 2002

Noone Peadar G, Zariwala Maimoona, Sannuti Aruna, Minnix Susan, Leigh Margaret W, Carson Johnny, Knowles Michael R

Abstract excerpt

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Share to Axonemal Dyneins
Share to Ciliary Motility Disorders
Share to Dyneins
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Polymorphism, Genetic

Share to Sequence Analysis, DNA

Source

Identifiers

PMID: 11893720

Genes

DNAI1

Provenance

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

Related research

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Research trail→

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Mutations in DNAI1 (IC78) cause primary ciliary dyskinesia.PMID 11893720Read ↗

<i>DNAI1</i> Mutations Explain Only 2% of Primary Ciliary DykinesiaSemantic proximity Read ↗

Mutations of DNAI1 in primary ciliary dyskinesia: evidence of founder effect in a common mutation.Semantic proximity Read ↗

Germline mutations in an intermediate chain dynein cause primary ciliary dyskinesia.Semantic proximity Read ↗

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

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

Primary ciliary dyskinesia caused by homozygous mutation in DNAL1, encoding dynein light chain 1.Semantic proximity Read ↗

Variation in DNAH1 may contribute to primary ciliary dyskinesia.Semantic proximity Read ↗

A novel genetic variant in DNAI2 detected by custom gene panel in a newborn with Primary Ciliary Dyskinesia: case report.Semantic proximity Read ↗

Deletions in DNAL1 Cause Primary Ciliary Dyskinesia Across North American Indigenous PopulationsSemantic proximity Read ↗

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

Identification of a novel founder variant in DNAI2 cause primary ciliary dyskinesia in five consanguineous families derived from a single tribe descendant of Arabian PeninsulaSemantic proximity Read ↗

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

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