Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome seq...
Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing
About this item
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Author / Creator
Publisher
United States: John Wiley & Sons, Inc
Journal title
Language
English
Formats
Publication information
Publisher
United States: John Wiley & Sons, Inc
Subjects
More information
Scope and Contents
Contents
The genetic heterogeneity of congenital hearing disorders makes molecular diagnosis expensive and time‐consuming using conventional techniques such as Sanger sequencing of DNA. In order to design an appropriate strategy of molecular diagnosis in the Algerian population, we explored the diversity of the involved mutations by studying 65 families aff...
Alternative Titles
Full title
Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing
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Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4444160
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4444160
Other Identifiers
ISSN
2324-9269
E-ISSN
2324-9269
DOI
10.1002/mgg3.131
