Prevalence of c.35delG and p.M34T mutations in the GJB2 gene in Estonia-Reference-Cited by-同舟云学术

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Prevalence of c.35delG and p.M34T mutations in the GJB2 gene in Estonia

Published:2010-09 Issue:9 Volume:74 Page:1007-1012
ISSN:0165-5876
Container-title:International Journal of Pediatric Otorhinolaryngology
language:en
Short-container-title:International Journal of Pediatric Otorhinolaryngology

Author:

Teek Rita,Kruustük Katrin,Zordania Riina,Joost Kairit,Reimand Tiia,Möls Tõnu,Oitmaa Eneli,Kahre Tiina,Tõnisson Neeme,Õunap Katrin

Funder

Eesti Teadusfondi

Haridus- ja Teadusministeerium

Publisher

Elsevier BV

Subject

Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health

Reference40 articles.

1. Genetic epidemiological studies of early-onset deafness in the U.S. School-age population;Marazita;Am. J. Med. Genet.,1993

2. Does universal newborn hearing screening identify all children with gjb2 (connexin 26) deafness? Penetrance of gjb2 deafness;Norris;Ear Hear.,2006

3. Non-syndromic, autosomal-recessive deafness;Petersen;Clin. Genet.,2006

4. A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q;Guilford;Nat. Genet.,1994

5. Forty-six genes causing nonsyndromic hearing impairment: Which ones should be analyzed in DNA diagnostics?;Hilgert;Mutat. Res.,2009

Cited by 18 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. Genetics of Hearing Impairment in North-Eastern Romania—A Cost-Effective Improved Diagnosis and Literature Review;Genes;2020-12-15

2. Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis;Proceedings of the National Academy of Sciences;2020-11-23

3. Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia;BMC Medical Genetics;2018-08-07

4. GJB2 and GJB6 genes mutations in children with non-syndromic hearing loss;Revista Romana de Medicina de Laborator;2017-02-18

5. Spectrum and Frequency of the GJB2 Gene Pathogenic Variants in a Large Cohort of Patients with Hearing Impairment Living in a Subarctic Region of Russia (the Sakha Republic);PLOS ONE;2016-05-25

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