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Article

DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia.

PLoS genetics - 1 Feb 2016

Li You, Yagi Hisato, Onuoha Ezenwa Obi, Damerla Rama Rao, Francis Richard, Furutani Yoshiyuki, Tariq Muhammad, King Stephen M, Hendricks Gregory, Cui Cheng, Saydmohammed Manush, Lee Dong Min, Zahid Maliha, Sami Iman, Leatherbury Linda, Pazour Gregory J, Ware Stephanie M, Nakanishi Toshio, Goldmuntz Elizabeth, Tsang Michael, Lo Cecilia W

Abstract excerpt

Heterotaxy, a birth defect involving left-right patterning defects, and primary ciliary dyskinesia (PCD), a sinopulmonary disease with dyskinetic/immotile cilia in the airway are seemingly disparate diseases. However, they have an overlapping genetic etiology involving mutations in cilia genes, a reflection of the common requirement for motile cilia in left-right patterning and airway clearance. While PCD is a...

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Source

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Identifiers

PMID: 26918822
DOI: 10.1371/journal.pgen.1005821
PMCID: PMC4769270

Genes

DNAH6
DNAI1
DNAH5

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia.PMID 26918822Read ↗

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