Elucidation of the unique mutation spectrum of severe hearing loss in a Vietnamese pediatric population-Reference-Cited by-同舟云学术

Elucidation of the unique mutation spectrum of severe hearing loss in a Vietnamese pediatric population

Published:2019-02-07 Issue:1 Volume:9 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Han Jae Joon,Nguyen Pham Dinh,Oh Doo-Yi,Han Jin Hee,Kim Ah-Reum,Kim Min Young,Park Hye-Rim,Tran Lam Huyen,Dung Nguyen Huu,Koo Ja-Won,Lee Jun Ho,Oh Seung Ha,Anh Vu Hoang,Choi Byung Yoon

Funder

Ministry of Education

Ministry of Health and Welfare

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/s41598-018-38245-4.pdf

Reference66 articles.

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2. Morton, C. C. & Nance, W. E. Newborn hearing screening–a silent revolution. N Engl J Med 354, 2151–2164, https://doi.org/10.1056/NEJMra050700 (2006).

3. Park, J. H. et al. Exploration of molecular genetic etiology for Korean cochlear implantees with severe to profound hearing loss and its implication. Orphanet J Rare Dis 9, 167, https://doi.org/10.1186/s13023-014-0167-8 (2014).

4. Wu, C. C., Lee, Y. C., Chen, P. J. & Hsu, C. J. Predominance of genetic diagnosis and imaging results as predictors in determining the speech perception performance outcome after cochlear implantation in children. Archives of pediatrics & adolescent medicine 162, 269–276, https://doi.org/10.1001/archpediatrics.2007.59 (2008).

5. Black, J., Hickson, L., Black, B. & Perry, C. Prognostic indicators in paediatric cochlear implant surgery: a systematic literature review. Cochlear implants international 12, 67–93, https://doi.org/10.1179/146701010x486417 (2011).

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