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Journal Abstract Search

238 related items for PubMed ID: 28819721

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  • 27. Novel compound heterozygous variants of SLC12A3 gene in a Chinese patient with Gitelman syndrome: a case report.
    Chen W, Zhou Q, Chen H, Li H, Chen J.
    Front Genet; 2023; 14():1067242. PubMed ID: 37377595
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  • 29. [Gitelman´s syndrome as common cause of hypokalemia and hypomagnesemia].
    Ryšavá R, Reiterová J, Urbanová M, Štekrová J, Lněnička P, Tesař V.
    Vnitr Lek; 2016; 62 Suppl 6():78-83. PubMed ID: 28124936
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  • 35. Gitelman Syndrome Provisionally Diagnosed During the First Presentation of Diabetic Ketoacidosis.
    Jalalzadeh M, Garcia Goncalves de Brito D, Chaudhari S, Poor AD, Baumstein D.
    Cureus; 2021 Apr 02; 13(4):e14253. PubMed ID: 33954067
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  • 37. A new mutation (intron 9 +1 G>T) in the SLC12A3 gene is linked to Gitelman syndrome in Gypsies.
    Coto E, Rodriguez J, Jeck N, Alvarez V, Stone R, Loris C, Rodriguez LM, Fischbach M, Seyberth HW, Santos F.
    Kidney Int; 2004 Jan 02; 65(1):25-9. PubMed ID: 14675033
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  • 39. Gitelman syndrome combined with complete growth hormone deficiency.
    Min SR, Cho HS, Hong J, Cheong HI, Ahn SY.
    Ann Pediatr Endocrinol Metab; 2013 Mar 02; 18(1):36-9. PubMed ID: 24904849
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  • 40. Simultaneous Homozygous Mutations in SLC12A3 and CLCNKB in an Inbred Chinese Pedigree.
    Mou L, Wu F.
    Genes (Basel); 2021 Mar 05; 12(3):. PubMed ID: 33807568
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