A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family.
Author:
Publisher
Elsevier BV
Subject
Genetics,General Medicine
Reference38 articles.
1. GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2-35delG mutation;Abidi;Int. J. Pediatr. Otorhinolaryngol.,2007
2. Carrier frequencies of mutations/polymorphisms in the connexin 26 gene (GJB2) in the Moroccan population;Abidi;Genet. Test.,2008
3. A method and server for predicting damaging missense mutations;Adzhubei;Nat. Methods,2010
4. Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing;Ammar-Khodja;Mol. Genet. Genomic Med.,2015
5. High frequency of the p.R34X mutation in the TMC1 gene associated with nonsyndromic hearing loss is due to founder effects;Ben Said;Genet. Test. Mol. Biomark.,2010
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1. Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Associated with Non-syndromic Deafness in Moroccan Families;Biochemical Genetics;2023-10-01
2. Functional consequences of Genetics variant in TMC1 and TMC2 within a United Arab Emirates family with Pre-lingual hearing loss;Saudi Journal of Biological Sciences;2023-02
3. A systematic review of the monogenic causes of Non‐Syndromic Hearing Loss (NSHL) and discussion of Current Diagnosis and Treatment options;Clinical Genetics;2022-09-29
4. Genetic heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB variants detected among hearing impaired families in Morocco;Molecular Biology Reports;2022-03-17
5. Hearing loss in Africa: current genetic profile;Human Genetics;2021-10-05
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