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Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto’s Thyroiditis Caused by Compound Heterozygous SLC12A3 Mutations

机译：对两种Gitelman综合征的少数复合蛋白尿或Hashimoto的甲状腺炎，复合杂合子SLC12A3突变引起的审查与分析

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Jian-hui Zhang; Dan-dan Ruan; Ya-nan Hu; Xing-lin Ruan; Yao-bin Zhu; Xiao Yang; Jia-bin Wu; Xin-fu Lin; Jie-wei Luo; Fa-qiang Tang;
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专利

1. Identification of compound mutations of SLC12A3 gene in a Chinese pedigree with Gitelman syndrome exhibiting Bartter syndrome-liked phenotypes [J] . Bingzi Dong, Ying Chen, Xinying Liu, BMC Nephrology . 2020,第1期

机译：鉴定吉特曼综合征展示Bartter综合征喜欢表型的Chinumigree中SLC12A3基因的复合突变
2. A novel compound heterozygous variant of the SLC12A3 gene in Gitelman syndrome pedigree [J] . Yixin Chen, Ziyi Zhang, Xihua Lin, BMC Medical Genetics . 2018,第1期

机译：Gitelman综合征谱系中SLC12A3基因的新型复合杂合变体
3. A NOVEL COMPOUND HETEROZYGOUS VARIANT OF SLC12A3 GENE IN A PEDIGREE WITH GITELMAN SYNDROME CO-EXISTENT WITH THYROID DYSFUNCTION [J] . Liu Simo, Ke Jing, Zhang Baoyu, Endocrine practice: official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists . 2018,第10期

机译：用甲状腺功能障碍与甲状腺功能障碍与甲状腺综合征共存的血小板综合征中的SLC12A3基因的一种新化合物杂合变体
4. Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimotos Thyroiditis Caused by Compound Heterozygous [O] . Jian-hui Zhang, Dan-dan Ruan, Ya-nan Hu, 2021

机译：对两种GITELMAN综合征群组合蛋白尿或哈希米多的甲状腺炎的审查与分析化合物杂合
5. Long-term Clinical Course after Living Kidney Donation by a Patient with Gitelman Syndrome Harboring a Compound Heterozygous Mutation of the SLC12A3 Gene [O] . Sahoko Kamejima, Izumi Yamamoto, Akiko Tajiri, 2021

机译：长期临床课程患有肾脏捐赠的肾脏捐赠，患有吉他人综合征，含有 SLC12A3 基因的化合物杂合突变

Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto’s Thyroiditis Caused by Compound Heterozygous SLC12A3 Mutations

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