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Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome

Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1815978273

Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome

About this item

Full title

Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome

Publisher

United States: Public Library of Science

Journal title

PloS one, 2016-09, Vol.11 (9), p.e0161893-e0161893

Language

English

Formats

Publication information

Publisher

United States: Public Library of Science

More information

Scope and Contents

Contents

Usher syndrome (USH) is an autosomal recessive disorder characterized by a dual sensory impairment affecting hearing and vision. USH is clinically and genetically heterogeneous. Ten different causal genes have been reported. We studied the molecular bases of the disease in 18 unrelated Algerian patients by targeted-exome sequencing, and identified...

Alternative Titles

Full title

Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_plos_journals_1815978273

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1815978273

Other Identifiers

ISSN

1932-6203

E-ISSN

1932-6203

DOI

10.1371/journal.pone.0161893

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