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LOF variants identifying candidate genes of laterality defects patients with congenital heart diseas...

LOF variants identifying candidate genes of laterality defects patients with congenital heart diseas...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_2766098380

LOF variants identifying candidate genes of laterality defects patients with congenital heart disease

About this item

Full title

LOF variants identifying candidate genes of laterality defects patients with congenital heart disease

Publisher

United States: Public Library of Science

Journal title

PLoS genetics, 2022-12, Vol.18 (12), p.e1010530-e1010530

Language

English

Formats

Publication information

Publisher

United States: Public Library of Science

More information

Scope and Contents

Contents

Defects in laterality pattern can result in abnormal positioning of the internal organs during the early stages of embryogenesis, as manifested in heterotaxy syndrome and situs inversus, while laterality defects account for 3~7% of all congenital heart defects (CHDs). However, the pathogenic mechanism underlying most laterality defects remains unkn...

Alternative Titles

Full title

LOF variants identifying candidate genes of laterality defects patients with congenital heart disease

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_plos_journals_2766098380

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_2766098380

Other Identifiers

ISSN

1553-7404,1553-7390

E-ISSN

1553-7404

DOI

10.1371/journal.pgen.1010530

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