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

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

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1773769573

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

About this item

Full title

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

Publisher

United States: Public Library of Science

Journal title

PLoS genetics, 2016-02, Vol.12 (2), p.e1005821

Language

English

Formats

Publication information

Publisher

United States: Public Library of Science

More information

Scope and Contents

Contents

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 cili...

Alternative Titles

Full title

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

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_plos_journals_1773769573

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1773769573

Other Identifiers

ISSN

1553-7404,1553-7390

E-ISSN

1553-7404

DOI

10.1371/journal.pgen.1005821

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