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(HYNCPEELE@kmaill.xyz)： 16 In humans, mutations in the claudin 16 previously known as paracellin 1 and claudin 19 genes cause a hereditary disease, familial hypomagnesemia with hypercalciuria and nephrocalcinosis FHHNC, which is characterized by excessive renal magnesium and calcium wasting, polyuria, recurrent urinary tract infections, bilateral nephrocalcinosis, and progressive kidney failure generic cialis2023/7/21 17:40:19 |
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