Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome
Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome
About this item
Full title
Author / Creator
Publisher
United States: Public Library of Science
Journal title
Language
English
Formats
Publication information
Publisher
United States: Public Library of Science
Subjects
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
Authors, Artists and Contributors
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