Study of the TMPRSS3 gene of patients with non-syndromic deafness
碩士 === 中山醫學大學 === 醫學研究所 === 95 === Hearing loss is the most common sensory defect in humans. The cause of this disease is multifactorial and includes both genetic and environmental factors. Non-syndromic autosomal recessive deafness accounts for about 70% cases of congenital hereditary hearing loss....
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| Format: | Others |
| Language: | zh-TW |
| Published: |
2007
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| Online Access: | http://ndltd.ncl.edu.tw/handle/94600412947492721540 |