Connexin gene mutations among ugandan patients with nonsyndromic sensorineural hearing loss-Reference-Cited by-同舟云学术

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Connexin gene mutations among ugandan patients with nonsyndromic sensorineural hearing loss

Published:2014-05-02 Issue:9 Volume:124 Page:E373-E376
ISSN:0023-852X
Container-title:The Laryngoscope
language:en
Short-container-title:The Laryngoscope

Author:

Javidnia Hedyeh¹,Carson Nancy²,Awubwa Michael³,Byaruhanga Richard³,Mack David⁴,Vaccani Jean-Philippe⁵

Affiliation:

1. Department of Otolaryngology, Head and Neck Surgery; The Ottawa Hospital; Ottawa Ontario Canada

2. Molecular Genetics and Diagnostics Laboratory; Children's Hospital of Eastern Ontario; Ottawa Ontario Canada

3. Department of ENT; Makerere University; Kampala Uganda

4. Department of Gastroenterology; Children's Hospital of Eastern Ontario; Ottawa Ontario Canada

5. Division of Otolaryngology, Department of Surgery; Children's Hospital of Eastern Ontario; Ottawa Ontario Canada

Publisher

Wiley

Subject

Otorhinolaryngology

Reference34 articles.

1. Hereditary sensorineural hearing loss: advances in molecular genetics and mutation analysis;Schrijver;Expert Rev Mol Diagn,2006

2. Genetic epidemiology of hearing impairment;Morton;Ann N Y Acad Sci,1991

3. http://hereditaryhearingloss.org

4. GJB2 (connexin 26) variants and nonsyndromic sensorineural hearing loss: a HuGE review;Kenneson;Genet Med,2002

Cited by 16 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. Whole exome sequencing reveals a biallelic frameshift mutation in GRXCR2 in hearing impairment in Cameroon;Molecular Genetics & Genomic Medicine;2021-02-02

2. Connexin Genes Variants Associated with Non-Syndromic Hearing Impairment: A Systematic Review of the Global Burden;Life;2020-10-28

3. Whole exome sequencing reveals pathogenic variants in MYO3A, MYO15A and COL9A3 and differential frequencies in ancestral alleles in hearing impairment genes among individuals from Cameroon;Human Molecular Genetics;2020-10-20

4. Hearing Impairment Overview in Africa: the Case of Cameroon;Genes;2020-02-22

5. GJB2 and GJB6 Mutations in Hereditary Recessive Non-Syndromic Hearing Impairment in Cameroon;Genes;2019-10-25

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