结论：HSF2基因多态性可能不是噪声性听力损失的遗传易感性因素。

Conclusion: Genetic polymorphism of the HSF2 gene might not be the susceptible factors of NIHL.

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目的探讨钙粘蛋白23基因(CDH23)多态性与噪声性听力损失之间的关系。

Objective To investigate the association of cadherin 23 gene (CDH23) polymorphisms with the development of noise induced hearing loss (NIHL).

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目的探讨谷胱甘肽硫转移酶M1和T1（GSTM1和GSTT1）的基因多态性与噪声性听力损失易感性之间的关系。

ObjectiveTo investigate the relationship of GSTM1 and GSTT1 gene polymorphisms with the development of noise induced hearing loss (NIHL) in Chinese workers.

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目的探讨质膜Ca2 +- ATP酶异构体2 （PMCA2 ）基因多态性与噪声性听力损失的关系。

Objective To investigate the association of plasma membrane Ca 2+ -ATPase isomer 2 gene(PMCA2)polymorphisms with the development of noise-induced hearing loss(NIHL).

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目的探讨质膜Ca2 +- ATP酶异构体2 （PMCA2 ）基因多态性与噪声性听力损失的关系。

Objective To investigate the association of plasma membrane Ca 2+ -ATPase isomer 2 gene(PMCA2)polymorphisms with the development of noise-induced hearing loss(NIHL).

youdao