The 342-kb deletion inGJB6is not present in patients with non-syndromic hearing loss from Austria-Reference-Cited by-同舟云学术

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The 342-kb deletion inGJB6is not present in patients with non-syndromic hearing loss from Austria

Published:2003-07-14 Issue:2 Volume:22 Page:180-180
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Günther Barbara,Steiner Andrea,Nekahm-Heis Doris,Albegger Klaus,Zorowka Patrick,Utermann Gerd,Janecke Andreas

Funder

Austrian Science Fund

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Cited by 28 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. GJB2 and GJB6 Genetic Variant Curation in an Argentinean Non-Syndromic Hearing-Impaired Cohort;Genes;2020-10-21

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

3. First report of prevalence c.IVS1+1G>A and del (GJB6-13S1854) mutations in Syrian families with non-syndromic sensorineural hearing loss;International Journal of Pediatric Otorhinolaryngology;2017-01

4. Investigation of the GJB6 Deletion Mutations Del (GJB6-D13s1830) and Del (GJB6-D13s1854) in Iranian Patients with Autosomal-Recessive Non-Syndromic Hearing Loss (ARNSHL);Brazilian Archives of Biology and Technology;2016

5. Spectrum of GJB2 mutations in Cypriot nonsyndromic hearing loss subjects;Journal of Genetics;2014-07-26

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