Update of the spectrum of GJB2 gene mutations in 152 Moroccan families with autosomal recessive nonsyndromic hearing loss.

[1]  C. Srisailapathy,et al.  Autosomal Dominant Hearing Loss resulting from p.R75Q Mutation in the GJB2 Gene: Nonsyndromic presentation in a South Indian Family , 2015, Annals of human genetics.

[2]  K. Kahrizi,et al.  Genetics of non-syndromic hearing loss in the Middle East. , 2014, International journal of pediatric otorhinolaryngology.

[3]  Yuan-yuan Zhang,et al.  R75Q de novo dominant mutation of GJB2 in a Chinese family with hearing loss and palmoplantar keratoderma. , 2014, International journal of pediatric otorhinolaryngology.

[4]  T. Strom,et al.  Genetic Spectrum of Autosomal Recessive Non-Syndromic Hearing Loss in Pakistani Families , 2014, PloS one.

[5]  J. Lasak,et al.  Hearing loss: diagnosis and management. , 2014, Primary care.

[6]  D. Chan,et al.  GJB2‐associated hearing loss: Systematic review of worldwide prevalence, genotype, and auditory phenotype , 2014, The Laryngoscope.

[7]  Guy Van Camp,et al.  Deafness and Hereditary Hearing Loss Overview , 2014 .

[8]  S. Abdelhak,et al.  Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing loss. , 2013, Gene.

[9]  W. Park,et al.  Prevalence of p.V37I Variant of GJB2 in Mild or Moderate Hearing Loss in a Pediatric Population and the Interpretation of Its Pathogenicity , 2013, PloS one.

[10]  T. Yang,et al.  The p.V37I Exclusive Genotype Of GJB2: A Genetic Risk-Indicator of Postnatal Permanent Childhood Hearing Impairment , 2012, PloS one.

[11]  H. Rehm,et al.  Molecular Diagnosis of Hearing Loss , 2012, Current protocols in human genetics.

[12]  A. Tessa,et al.  Molecular Investigation of Pediatric Portuguese Patients with Sensorineural Hearing Loss , 2011, Genetics research international.

[13]  Richard J. H. Smith,et al.  Function and expression pattern of nonsyndromic deafness genes. , 2009, Current molecular medicine.

[14]  B. Wu,et al.  GJB2 mutation spectrum in 2063 Chinese patients with nonsyndromic hearing impairment , 2009, Journal of Translational Medicine.

[15]  Richard J. H. Smith,et al.  Forty-six genes causing nonsyndromic hearing impairment: which ones should be analyzed in DNA diagnostics? , 2009, Mutation research.

[16]  H. Rouba,et al.  The analysis of three markers flanking GJB2 gene suggests a single origin of the most common 35delG mutation in the Moroccan population. , 2008, Biochemical and biophysical research communications.

[17]  H. Rouba,et al.  Carrier frequencies of mutations/polymorphisms in the connexin 26 gene (GJB2) in the Moroccan population. , 2008, Genetic testing.

[18]  Hong-Joon Park,et al.  Carrier frequency of GJB2 (connexin-26) mutations causing inherited deafness in the Korean population , 2008, Journal of Human Genetics.

[19]  H. Rouba,et al.  GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2-35delG mutation. , 2007, International journal of pediatric otorhinolaryngology.

[20]  B. Han,et al.  The prevalence of the 235delC GJB2 mutation in a Chinese deaf population , 2007, Genetics in Medicine.

[21]  Mustafa Tekin,et al.  GJB2 mutations and degree of hearing loss: a multicenter study. , 2005, American journal of human genetics.

[22]  C. Petit,et al.  GJB2 and GJB6 mutations: genotypic and phenotypic correlations in a large cohort of hearing-impaired patients. , 2005, Archives of otolaryngology--head & neck surgery.

[23]  M. Tekin,et al.  Evidence for single origins of 35delG and delE120 mutations in the GJB2 gene in Anatolia , 2004, Clinical genetics.

[24]  H. Rehm Molecular Diagnosis of Hearing Loss , 2004, Current protocols in human genetics.

[25]  B. Wollnik,et al.  The novel R75Q mutation in the GJB2 gene causes autosomal dominant hearing loss and palmoplantar keratoderma in a Turkish family , 2002, Clinical genetics.

[26]  D. Yannoukakos,et al.  Prelingual Nonsyndromic Hearing Loss in Greece , 2002, ORL.

[27]  A Martini,et al.  Exploring the clinical and epidemiological complexity of GJB2-linked deafness. , 2002, American journal of medical genetics.

[28]  G. Utermann,et al.  Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with GJB2 mutations – phenotypic spectrum and frequencies of GJB2 mutations in Austria , 2002, Human Genetics.

[29]  E. Sartorato,et al.  Deafness resulting from mutations in the GJB2 (connexin 26) gene in Brazilian patients , 2002, Clinical genetics.

[30]  C. Petit,et al.  Autosomal recessive non-syndromic hearing loss in the Lebanese population: prevalence of the 30delG mutation and report of two novel mutations in the connexin 26 (GJB2) gene , 2001, Journal of medical genetics.

[31]  W. Kimberling,et al.  Prevalent connexin 26 gene (GJB2) mutations in Japanese , 2000, Journal of medical genetics.

[32]  F. Zacchello,et al.  Cx26 deafness: mutation analysis and clinical variability , 1999, Journal of medical genetics.

[33]  H. Hibino,et al.  Three novel connexin26 gene mutations in autosomal recessive non-syndromic deafness. , 1999, Neuroreport.

[34]  H. Ostrer,et al.  Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness. , 1998, The New England journal of medicine.

[35]  J. W. Askew,et al.  Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss. , 1998, American journal of human genetics.

[36]  F. Ammar-Khodja,et al.  Frequency of the 35delG allele causing nonsyndromic recessive deafness in the Algerian patients. , 2007, Genetic counseling.

[37]  F. Razjou,et al.  Evaluation of the Correct Use of Virkon Disinfectant in Reducing Bacterial Contamination of Platelets Components Prepared , 2007 .

[38]  M. Patton,et al.  Familial and sporadic GJB2-related deafness in iran: Review of gene mutations , 2007 .

[39]  X. Estivill,et al.  Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene. , 2000 .