Study of the Connexin29 genePart I Expression of gap junction protein connexin29 in the adult mouse cochlea Part II Mutation and functional study of Cx29 gene in prelingual nonsyndromic sensorineural deafness
碩士 === 中山醫學大學 === 醫學研究所 === 93 === Hearing loss is one of the most common sensorineural diseases. The incidence of this profound prelingual deafness is approximately one per 1000 at birth. The cause of this disease includes many genetic and environmental factors, or both. Understanding of the geneti...
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| Format: | Others |
| Language: | zh-TW |
| Published: |
2005
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| Online Access: | http://ndltd.ncl.edu.tw/handle/16469206359758241919 |