Molecular analysis of the TMPRSS3 gene in Moroccan families with non-syndromic hearing loss-Reference-Cited by-同舟云学术

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Molecular analysis of the TMPRSS3 gene in Moroccan families with non-syndromic hearing loss

Published:2012-03 Issue:4 Volume:419 Page:643-647
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Charif Majida,Abidi Omar,Boulouiz Redouane,Nahili Halima,Rouba Hassan,Kandil Mostafa,Delprat Benjamin,Lenaers Guy,Barakat Abdelhamid

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference31 articles.

1. Molecular genetics of hearing loss;Petit;Annu. Rev. Genet.,2001

2. Molecular genetics of hearing impairment due to mutations in gap junction genes encoding beta connexins;Rabionet;Hum. Mutat.,2000

3. Absence of GJB2 gene mutations, the GJB6 deletion (GJB6-D13S1830) and four common mitochondrial mutations in non syndromic genetic hearing loss in a South African population;Kabahuma;Int. J. Pediatr. Otorhinolaryngol.,2011

4. Hereditary non-syndromic sensorineural hearing loss: transforming silence to sound;Schrijver;J. Mol. Diagn.,2004

5. Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3;Bonne-Tamir;Am. J. Hum. Genet.,1996

Cited by 15 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Genotype-Phenotype Correlations in TMPRSS3 (DFNB10/DFNB8) with Emphasis on Natural History;Audiology and Neurotology;2023

2. TMPRSS3 Gene Variants With Implications for Auditory Treatment and Counseling;Frontiers in Genetics;2021-11-19

3. Genetics and meta-analysis of recessive non-syndromic hearing impairment and Usher syndrome in Maghreb population: lessons from the past, contemporary actualities and future challenges;Human Genetics;2021-07-15

4. A novel pathogenic variant in the LRTOMT gene causes autosomal recessive non-syndromic hearing loss in an Iranian family;BMC Medical Genetics;2020-06-09

5. Long non‑coding RNA EBLN3P promotes the recovery of the function of impaired spiral ganglion neurons by competitively binding to miR‑204‑5p and regulating TMPRSS3 expression;International Journal of Molecular Medicine;2020-03-17

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