Functional analysis of the CX30.2/CX31.3 gene
碩士 === 中山醫學大學 === 生物醫學科學學系碩士班 === 98 === Connexins (CXs) are known to be involved in human nonsyndromic genetic deafness. Among a cohort of patients with nonsyndromic hearing loss, we recently identified novel heterozygous missense mutation, p.R15G, p.L23H and p.W77S, in the GJC3 gene encoding CX30....
| Main Authors: | , |
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| Other Authors: | |
| Format: | Others |
| Language: | zh-TW |
| Published: |
2010
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| Online Access: | http://ndltd.ncl.edu.tw/handle/75312862783113430505 |