Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Hypophosphatemia and SLC34A1[original query] |
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Renal phosphate handling and inherited disorders of phosphate reabsorption: an update. Pediatric nephrology (Berlin, Germany) 2017 12 34 (4): 549-559. Wagner Carsten A, Rubio-Aliaga Isabel, Hernando Na |
Clinical aspects of the phosphate transporters NaPi-IIa and NaPi-IIb: mutations and disease associations. Pflugers Archiv : European journal of physiology 2018 12 471 (1): 137-148. Lederer Eleanor, Wagner Carsten |
The genetic polymorphisms of XPR1 and SCL34A3 are associated with Fanconi syndrome in Chinese patients of tumor-induced osteomalacia. Journal of endocrinological investigation 2020 Jul . Jiang Y, Li X, Feng J, Li M, Wang O, Xing X-P, Xia W |
Overlapping Phenotypes Associated With CYP24A1, SLC34A1, and SLC34A3 Mutations: A Cohort Study of Patients With Hypersensitivity to Vitamin D. Frontiers in endocrinology 2021 11 12 736240. Molin Arnaud, Lemoine Sandrine, Kaufmann Martin, Breton Pierre, Nowoczyn Marie, Ballandonne Céline, Coudray Nadia, Mittre Hervé, Richard Nicolas, Ryckwaert Amélie, Lavillaureix Alinoe, Jones Glenville, Bacchetta Justine, Kottler Marie-Lau |
Idiopathic infantile hypercalcemia in children with chronic kidney disease due to kidney hypodysplasia. Pediatric nephrology (Berlin, Germany) 2022 9 38 (4): 1067-1073. Gurevich Evgenia, Borovitz Yael, Levi Shelli, Perlman Sharon, Landau Dani |
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- Page last updated:Apr 16, 2024
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