Exploration of molecular genetic etiology for Korean cochlear implantees with severe to profound hearing loss and its implication-Reference-Cited by-同舟云学术

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Exploration of molecular genetic etiology for Korean cochlear implantees with severe to profound hearing loss and its implication

Published:2014-11-06 Issue:1 Volume:9 Page:
ISSN:1750-1172
Container-title:Orphanet Journal of Rare Diseases
language:en
Short-container-title:Orphanet J Rare Dis

Author:

Park Joo Hyun,Kim Nayoung K D,Kim Ah Reum,Rhee Jihye,Oh Seung Ha,Koo Ja-Won,Nam Jae-Yong,Park Woong-Yang,Choi Byung Yoon

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics(clinical),General Medicine

Link

http://link.springer.com/content/pdf/10.1186/s13023-014-0167-8.pdf

Reference60 articles.

1. Varga L, Masindova I, Huckova M, Kabatova Z, Gasperikova D, Klimes I, Profant M: Prevalence of DFNB1 mutations among cochlear implant users in Slovakia and its clinical implications. Eur Archives Otorhinolaryngol. 2014, 271 (6): 1401-1407. 10.1007/s00405-013-2559-0.

2. Wu CC, Liu TC, Wang SH, Hsu CJ, Wu CM: Genetic characteristics in children with cochlear implants and the corresponding auditory performance. Laryngoscope. 2011, 121 (6): 1287-1293. 10.1002/lary.21751.

3. Miyagawa M, Naito T, Nishio SY, Kamatani N, Usami S: Targeted exon sequencing successfully discovers rare causative genes and clarifies the molecular epidemiology of Japanese deafness patients. PLoS One. 2013, 8: e71381-10.1371/journal.pone.0071381.

4. Joshi VM, Navlekar SK, Kishore GR, Reddy KJ, Kumar EC: CT and MR imaging of the inner ear and brain in children with congenital sensorineural hearing loss. Radiographics. 2012, 32: 683-698. 10.1148/rg.323115073.

5. Elziere M, Roman S, Nicollas R, Triglia JM: Value of systematic aetiological investigation in children with sensorineural hearing loss. Eur Ann Otorhinolaryngol Head Neck Dis. 2012, 129: 185-189. 10.1016/j.anorl.2011.05.009.

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