GJB2 Mutations in Patients with Nonsyndromic Hearing Loss from Croatia-Reference-Cited by-同舟云学术

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GJB2 Mutations in Patients with Nonsyndromic Hearing Loss from Croatia

Published:2009-10 Issue:5 Volume:13 Page:693-699
ISSN:1945-0265
Container-title:Genetic Testing and Molecular Biomarkers
language:en
Short-container-title:Genetic Testing and Molecular Biomarkers

Author:

Sansović Ivona¹,Knežević Jelena²,Musani Vesna²,Seeman Pavel³,Barišić Ingeborg¹,Pavelić Jasminka²

Affiliation:

1. Department of Pediatrics, Children's Hospital Zagreb, University of Zagreb, Medical School, Zagreb, Croatia.

2. Division of Molecular Medicine, Rudjer Boškovic Institute, Zagreb, Croatia.

3. Department of Child Neurology, Charles University Prague, Prague, Czech Republic.

Publisher

Mary Ann Liebert Inc

Subject

Genetics(clinical),General Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/gtmb.2009.0073

Reference42 articles.

1. Prevalent connexin 26 gene (GJB2) mutations in Japanese

2. GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2–35delG mutation

3. High prevalence of theW24X mutation in the gene encoding connexin-26 (GJB2) in Spanish Romani (gypsies) with autosomal recessive non-syndromic hearing loss

4. A genotype-phenotype correlation for GJB2 (connexin 26) deafness

5. Prevalence and Evolutionary Origins of the del(GJB6-D13S1830) Mutation in the DFNB1 Locus in Hearing-Impaired Subjects: a Multicenter Study

Cited by 26 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. Spectrum of genetic variants in 306 patients with non-syndromic hearing loss from Croatia;Croatian Medical Journal;2024-06

2. Exome sequencing identifies novel variants associated with non-syndromic hearing loss in the Iranian population;PLOS ONE;2023-08-10

3. Genetic etiology of non-syndromic hearing loss in Europe;Human Genetics;2022-01-19

4. Etiologies of Childhood Hearing Impairment in Schools for the Deaf in Mali;Frontiers in Pediatrics;2021-11-29

5. GJB2 mutations in Iranian Azeri population with autosomal recessive nonsyndromic hearing loss (ARNSHL): First report of c.238 C>A mutation in Iran;Journal of Clinical Laboratory Analysis;2021-09-28

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