Connexin 26 mutations and nonsyndromic hearing impairment in Northern Finland-Reference-Cited by-同舟云学术

Connexin 26 mutations and nonsyndromic hearing impairment in Northern Finland

Published:2010-09-03 Issue:10 Volume:113 Page:1758-1763
ISSN:0023-852X
Container-title:The Laryngoscope
language:en
Short-container-title:The Laryngoscope

Author:

Löppönen Tuija,Väisänen Marja-Leena,Luotonen Mirja,Allinen Minna,Uusimaa Johanna,Lindholm PÄIvi,Mäki-Torkko Elina,Väyrynen Mirja,Löppönen Heikki,Leisti Jaakko

Publisher

Wiley

Subject

Otorhinolaryngology

Reference37 articles.

1. Prelingual deafness: high prevalence of 30delG mutation in the connexin 26 gene;Denoyelle;Hum Mol Genet,1997

2. Connexin-26 mutation in sporadic and inherited sensorineural deafness;Estivill;Lancet,1998

3. Novel mutations in connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss;Kelley;Am J Hum Genet,1998

4. Hearing loss;Nadol;N Engl J Med,1993

5. Epidemiology of permanent childhood hearing impairment in Trent Region, 1985-1993;Fortnum;Br J Audiol,1997

Cited by 29 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. Exome sequencing identifies novel variants associated with non-syndromic hearing loss in the Iranian population;PLOS ONE;2023-08-10

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

3. 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

4. Update of spectrum c.35delG and c.‐23+1G>A mutations on the GJB2 gene in individuals with autosomal recessive nonsyndromic hearing loss;Annals of Human Genetics;2018-09-03

5. GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants;International Journal of Pediatric Otorhinolaryngology;2018-04