Gitelman综合征SLC12A3基因突变功能验证及mRNA剪接异常突变机制研究
序号 | 标题 | 类型 | 作者 |
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1 | Functional Characterization of PHEX Gene Variants in Children With X-Linked Hypophosphatemic Rickets Shows No Evidence of Genotype-Phenotype Correlation | 期刊论文 | Zheng Bixia;Wang Chunli;Chen Qiuxia;Che Ruochen;Sha Yugen;Zhao Fei;Ding Guixia;Zhou Wei;Jia Zhanjun;Huang Songming;Chen Ying;Zhang Aihua |
2 | Splicing Characterization of CLCNKB Variants in Four Patients With Type III Bartter Syndrome | 期刊论文 | Wang Chunli;Han Yuan;Zhou Jiaran;Zheng Bixia;Zhou Wei;Bao Huaying;Jia Zhanjun;Zhang Aihua;Huang Songming;Ding Guixia;Zhao Fei |