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260 related items for PubMed ID: 30413979

  • 1. Characteristics and Follow-Up of 13 pedigrees with Gitelman syndrome.
    Zhong F, Ying H, Jia W, Zhou X, Zhang H, Guan Q, Xu J, Fang L, Zhao J, Xu C.
    J Endocrinol Invest; 2019 Jun; 42(6):653-665. PubMed ID: 30413979
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  • 2. Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto's Thyroiditis Caused by Compound Heterozygous SLC12A3 Mutations.
    Zhang JH, Ruan DD, Hu YN, Ruan XL, Zhu YB, Yang X, Wu JB, Lin XF, Luo JW, Tang FQ.
    Biomed Res Int; 2021 Jun; 2021():9973161. PubMed ID: 34046503
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  • 3. A novel compound heterozygous mutation of SLC12A3 gene in a pedigree with Gitelman syndrome and literature review.
    Yang M, Dong Y, Tian J, Yan L, Chen Y, Qiu H, Liu W, Hu Y.
    Genes Genomics; 2020 Sep; 42(9):1035-1040. PubMed ID: 32712837
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  • 12. A pedigree analysis of two homozygous mutant Gitelman syndrome cases.
    Luo J, Yang X, Liang J, Li W.
    Endocr J; 2015 Sep; 62(1):29-36. PubMed ID: 25273610
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  • 13. [Clinical and genetic characteristics of Gitelman syndrome in 5 pedigrees].
    Shi RR, Li CC, Fang L, Xu J, Guan QB, Zhou XL, Guo J, Han WX, Chen Q, Feng L, Zhao JJ, Xu C.
    Zhonghua Nei Ke Za Zhi; 2017 Feb 01; 56(2):104-111. PubMed ID: 28162179
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