gene].

Lin Chung Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2021 Mar;35(3):229-233;237. doi:10.13201/j.issn.2096-7993.2021.03.008

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摘要

The next generation sequencing technology were used to screen the pathogenic gene mutation of inherited deafness. Combined with the genetic sequencing results of parents, the specific pathogenic gene mutation of deafness patients can be identified. While the pathogenicity of complex heterozygous mutation were explained by various pathogenicity analysis methods.

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