Literature DB >> 12408079

Clinical manifestations of DFNB29 deafness.

Zubair M Ahmed1, Saima Riazuddin, Thomas B Friedman, Sheikh Riazuddin, Edward R Wilcox, Andrew J Griffith.   

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Year:  2002        PMID： 12408079     DOI： 10.1159/000066828

Source DB:  PubMed          Journal:  Adv Otorhinolaryngol        ISSN： 0065-3071


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  4 in total

1.  Novel CLDN14 mutations in Pakistani families with autosomal recessive non-syndromic hearing loss.

Authors:  Kwanghyuk Lee; Muhammad Ansar; Paula B Andrade; Bushra Khan; Regie Lyn P Santos-Cortez; Wasim Ahmad; Suzanne M Leal
Journal:  Am J Med Genet A       Date:  2012-01-13       Impact factor: 2.802

2.  Mutations in CLDN14 are associated with different hearing thresholds.

Authors:  Rasheeda Bashir; Amara Fatima; Sadaf Naz
Journal:  J Hum Genet       Date:  2010-09-02       Impact factor: 3.172

3.  Phenotypic variability of CLDN14 mutations causing DFNB29 hearing loss in the Pakistani population.

Authors:  Zil-e-Huma Bashir; Noreen Latief; Inna A Belyantseva; Farheena Iqbal; S Amer Riazuddin; Sheikh Amer Riazuddin; Shaheen N Khan; Thomas B Friedman; Sheikh Riazuddin; Saima Riazuddin
Journal:  J Hum Genet       Date:  2012-12-13       Impact factor: 3.172

Review 4.  Molecular genetics of non-syndromic deafness.

Authors:  Vânia B Piatto; Ellen C T Nascimento; Fabiana Alexandrino; Camila A Oliveira; Ana Cláudia P Lopes; Edi Lúcia Sartorato; José Victor Maniglia
Journal:  Braz J Otorhinolaryngol       Date:  2005-08-02
  4 in total

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