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International Journal of Audiology Volume 51, 2012 - Issue 6
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Research Article

GJB2 (Connexin-26) mutations are not frequent among hearing impaired patients in East Greenland

Preben Homøe *Department of Otolaryngology, Head & Neck Surgery, Rigshospitalet, Copenhagen, DenmarkCorrespondence[email protected]
,
Anders KochDepartment of Epidemiology Research, Statens Serum Institut, Copenhagen, Denmark
,
Nanna Dahl RendtorffWilhelm Johannsen Centre for Functional Genome Research, Department of Cellular and Molecular Medicine, ICMM, University of Copenhagen, Denmark
,
Marianne LodahlWilhelm Johannsen Centre for Functional Genome Research, Department of Cellular and Molecular Medicine, ICMM, University of Copenhagen, Denmark
,
Ture AndersenDepartment of Audiology, Odense University Hospital, Denmark
,
Stig AndersenDepartment of Endocrinology, Aalborg Hospital, Denmark
,
Hans EibergWilhelm Johannsen Centre for Functional Genome Research, Department of Cellular and Molecular Medicine, ICMM, University of Copenhagen, Denmark
,
Inge-Merete NielsenWilhelm Johannsen Centre for Functional Genome Research, Department of Cellular and Molecular Medicine, ICMM, University of Copenhagen, Denmark
&
Lisbeth TranebjærgWilhelm Johannsen Centre for Functional Genome Research, Department of Cellular and Molecular Medicine, ICMM, University of Copenhagen, Denmark;Department of Audiology, Bispebjerg Hospital, Copenhagen, Denmark
 show all
Pages 433-436 | Received 12 Jan 2012, Accepted 20 Jan 2012, Published online: 27 Feb 2012

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Pál Weihe, Fróði Debes, Jónrit Halling, Maria Skaalum Petersen, Gina Muckle, Jon Øyvind Odland, Alexey A. Dudarev, Pierre Ayotte, Éric Dewailly, Philippe Grandjean & Eva Bonefeld-Jørgensen. (2016) Health effects associated with measured levels of contaminants in the Arctic. International Journal of Circumpolar Health 75:1.
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Jie Chen, Qinjun Wei, Jun Yao, Xiaoyun Qian, Yanhong Dai, Ye Yang, Xin Cao & Xia Gao. (2013) Identification of two heterozygous deafness mutations in SLC26A4 (PDS) in a Chinese family with two siblings. International Journal of Audiology 52:2, pages 134-138.
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Alan J. Parkinson. (2013) The Arctic Human Health Initiative: a legacy of the International Polar Year 2007–2009. International Journal of Circumpolar Health 72:1.
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Articles from other publishers (6)

Nikolay A. Barashkov, Vera G. Pshennikova, Olga L. Posukh, Fedor M. Teryutin, Aisen V. Solovyev, Leonid A. Klarov, Georgii P. Romanov, Nyurgun N. Gotovtsev, Andrey A. Kozhevnikov, Elena V. Kirillina, Oksana G. Sidorova, Lena M. Vasilyevа, Elvira E. Fedotova, Igor V. Morozov, Alexander A. Bondar, Natalya A. Solovyevа, Sardana K. Kononova, Adyum M. Rafailov, Nikolay N. Sazonov, Anatoliy N. Alekseev, Mikhail I. Tomsky, Lilya U. Dzhemileva, Elza K. Khusnutdinova & Sardana A. Fedorova. (2016) 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 11:5, pages e0156300.
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Keita Tsukada, Shin-ya Nishio, Mitsuru Hattori & Shin-ichi Usami. (2015) Ethnic-Specific Spectrum of GJB2 and SLC26A4 Mutations . Annals of Otology, Rhinology & Laryngology 124:1_suppl, pages 61S-76S.
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Guille García Sánchez, Alfonso Alfaro-Rodríguez & Adrián Poblano. (2014) Evidence for Central Asian Origin of the p.Val27Ile Variant in the GJB2 Gene . International Journal of Medical Genetics 2014, pages 1-8.
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Francisco Loeza-Becerra, María del Refugio Rivera-Vega, Mirna Martínez-Saucedo, Luz María Gonzalez-Huerta, Héctor Urueta-Cuellar, Pedro Berrruecos-Villalobos & Sergio Cuevas-Covarrubias. (2014) Particular distribution of the GJB2/GJB6 gene mutations in Mexican population with hearing impairment. International Journal of Pediatric Otorhinolaryngology 78:7, pages 1057-1060.
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Dylan K. Chan & Kay W. Chang. (2014) GJB2-associated hearing loss: Systematic review of worldwide prevalence, genotype, and auditory phenotype. The Laryngoscope 124:2, pages E34-E53.
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Xiaoming Wei, Yan Sun, Jiansheng Xie, Quan Shi, Ning Qu, Guanghui Yang, Jun Cai, Yi Yang, Yu Liang, Wei Wang & Xin Yi. (2012) Next-generation sequencing identifies a novel compound heterozygous mutation in MYO7A in a Chinese patient with Usher Syndrome 1B. Clinica Chimica Acta 413:23-24, pages 1866-1871.
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