Identification of a novel CDH23 gene variant associated with non-syndromic progressive hearing loss in a Chinese family: Individualized hearing rehabilitation guided by genetic diagnosis. (December 2019)

Record Type:: Journal Article
Title:: Identification of a novel CDH23 gene variant associated with non-syndromic progressive hearing loss in a Chinese family: Individualized hearing rehabilitation guided by genetic diagnosis. (December 2019)
Main Title:: Identification of a novel CDH23 gene variant associated with non-syndromic progressive hearing loss in a Chinese family: Individualized hearing rehabilitation guided by genetic diagnosis
Authors:: Chen, Ying
Li, Yun
Ren, Yan
Li, Haifeng
Huang, Meiping
Jia, Huan
Yang, Tao
Wang, Zhaoyan
Huang, Zhiwu
Wu, Hao
Abstract:
Is Part Of:: International journal of pediatric otorhinolaryngology. Volume 127(2019:Dec.)
Journal:: International journal of pediatric otorhinolaryngology
Issue:: Volume 127(2019:Dec.)
Issue Display:: Volume 127 (2019)
Year:: 2019
Volume:: 127
Issue Sort Value:: 2019-0127-0000-0000
Page Start:
Page End:
Publication Date:: 2019-12
Subjects:: Non-syndromic hearing loss -- Progressive hearing loss -- CDH23 -- Genetic diagnosis -- Hearing rehabilitation
Otolaryngology -- Periodicals
Pediatrics -- Periodicals
Otolaryngology -- Periodicals
Pediatrics -- Periodicals
Oto-rhino-laryngologie -- Périodiques
Pédiatrie -- Périodiques
618.9209751
Journal URLs:: http://www.sciencedirect.com/science/journal/01655876 ↗
http://www.elsevier.com/journals ↗
DOI:: 10.1016/j.ijporl.2019.109649 ↗
Languages:: English
ISSNs:: 0165-5876
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 4542.451000
British Library DSC - BLDSS-3PM
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Ingest File:: 23152.xml