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34878901 | Novel CUL3 Variant Causing Familial Hyperkalemic Hypertension Impairs Regulation and Function of Ubiquitin Ligase Activity. | 2022 Jan |
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| 2 |
35093948 | A Novel Homozygous KLHL3 Mutation as a Cause of Autosomal Recessive Pseudohypoaldosteronism Type II Diagnosed Late in Life. | 2022 Jan 28 |
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| 3 |
29848507 | The Calcium-Sensing Receptor Increases Activity of the Renal NCC through the WNK4-SPAK Pathway. | 2018 Jul |
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24266877 | Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome). | 2014 May |
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