Prevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss

Prevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss

Abstract Background To date, 102 genes have been reported as responsible for non-syndromic hearing loss, some of which are associated with specific audiogram features. Four genes have been reported as causative for mid-frequency sensorineural hearing loss (MFSNHL), among which TECTA is the most freq...

Full description

Bibliographic Details
Main Authors: Nobuko Yamamoto, Hideki Mutai, Kazunori Namba, Noriko Morita, Shin Masuda, Yasuyuki Nishi, Atsuko Nakano, Sawako Masuda, Masato Fujioka, Kimitaka Kaga, Kaoru Ogawa, Tatsuo Matsunaga
Format: Article
Language:English
Published: BMC 2017-09-01
Series:Orphanet Journal of Rare Diseases
Subjects:
DFNA8/12
DFNB21
TECTA
Mid-frequency hearing loss
Online Access:http://link.springer.com/article/10.1186/s13023-017-0708-z

Internet

http://link.springer.com/article/10.1186/s13023-017-0708-z

Similar Items