Study of TMIE and MYOSIN VIIA Genes of patients with nonsyndromic hearing loss in Taiwan
博士 === 中山醫學大學 === 醫學研究所 === 96 === In the developed countries, the incidence of congenital hearing loss is estimated at 1 in 1000 births, of which approximately 60% cases are attributed to genetic factors. To date, 59 auditory genes have been identified, some of which are those involved in K+ recycl...
Main Authors: | Mao-Chang, 蘇茂昌 |
---|---|
Other Authors: | 李宣佑 |
Format: | Others |
Language: | zh-TW |
Published: |
2008
|
Online Access: | http://ndltd.ncl.edu.tw/handle/02439699126590627758 |
Similar Items
-
Genetics of Nonsyndromic Congenital Hearing Loss
by: Oguz Kadir Egilmez, et al.
Published: (2016-01-01) -
Screening of Connexin 26 in Nonsyndromic Hearing Loss
by: Danielle Moreira, et al.
Published: (2015-01-01) -
Novel Mutations in the TMPRSS3 Gene May Contribute to Taiwanese Patients with Nonsyndromic Hearing Loss
by: Swee-Hee Wong, et al.
Published: (2020-03-01) -
Sequence variants in genes causing nonsyndromic hearing loss in a Pakistani cohort
by: Amjad Khan, et al.
Published: (2019-09-01) -
Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing Loss.
by: Tahir Atik, et al.
Published: (2015-01-01)