The first compound heterozygous mutations in SLC12A3 and PDX1 genes: a unique presentation of Gitelman syndrome with distinct insulin resistance and familial diabetes insights

Overview of attention for article published in Frontiers in endocrinology, January 2024

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RT @FrontEndocrinol: New Research: The first compound heterozygous mutations in SLC12A3 and PDX1 genes: a unique presentation of Gitelman s…

26 Jan 2024

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New Research: The first compound heterozygous mutations in SLC12A3 and PDX1 genes: a unique presentation of Gitelman syndrome with distinct insulin resistance and familial diabetes insights: Background Gitelman Syndrome (GS)… https://t.co/ON20COGPNh #Endo

25 Jan 2024

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