Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Hypophosphatemia and FGF23[original query] |
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A functional allelic variant of the FGF23 gene is associated with renal phosphate leak in calcium nephrolithiasis. The Journal of clinical endocrinology and metabolism 2012 May 97 (5): E840-4. Rendina Domenico, Esposito Teresa, Mossetti Giuseppe, De Filippo Gianpaolo, Gianfrancesco Fernando, Perfetti Anna, Magliocca Sara, Formisano Pietro, Prié Dominique, Strazzullo Pasqua |
Outcome of adult patients with X-linked hypophosphatemia caused by PHEX gene mutations. Journal of inherited metabolic disease 2018 2 41 (5): 865-876. Chesher Douglas, Oddy Michael, Darbar Ulpee, Sayal Parag, Casey Adrian, Ryan Aidan, Sechi Annalisa, Simister Charlotte, Waters Aoife, Wedatilake Yehani, Lachmann Robin H, Murphy Elai |
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 |
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