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SLC12A1
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Novel SLC12A1 mutations cause Bartter syndrome in two patients with different prognoses.
Functional characterization of SLC12A1 gene variants in 3 patients with Bartter syndrome type Ⅰ].
Ubiquitination of NKCC2 by the cullin-RING E3 ubiquitin ligase family in the thick ascending limb of…
Association of polymorphisms of calcium reabsorption genes SLC12A1, KCNJ1 and SLC8A1 with colorectal…
Generation of an induced pluripotent stem cell line from a Bartter syndrome patient with the homozyg…
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Renal Allograft Fibrosis Study
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