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Year | Number of Results |
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2002 | 1 |
2010 | 1 |
2015 | 1 |
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Nephrolithiasis and osteoporosis associated with hypophosphatemia caused by mutations in the type 2a sodium-phosphate cotransporter.
N Engl J Med. 2002 Sep 26;347(13):983-91. doi: 10.1056/NEJMoa020028.
N Engl J Med. 2002.
PMID: 12324554
Free article.
A loss-of-function mutation in NaPi-IIa and renal Fanconi's syndrome.
Magen D, Berger L, Coady MJ, Ilivitzki A, Militianu D, Tieder M, Selig S, Lapointe JY, Zelikovic I, Skorecki K.
Magen D, et al.
N Engl J Med. 2010 Mar 25;362(12):1102-9. doi: 10.1056/NEJMoa0905647.
N Engl J Med. 2010.
PMID: 20335586
Free article.
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Autosomal-Recessive Mutations in SLC34A1 Encoding Sodium-Phosphate Cotransporter 2A Cause Idiopathic Infantile Hypercalcemia.
Schlingmann KP, Ruminska J, Kaufmann M, Dursun I, Patti M, Kranz B, Pronicka E, Ciara E, Akcay T, Bulus D, Cornelissen EA, Gawlik A, Sikora P, Patzer L, Galiano M, Boyadzhiev V, Dumic M, Vivante A, Kleta R, Dekel B, Levtchenko E, Bindels RJ, Rust S, Forster IC, Hernando N, Jones G, Wagner CA, Konrad M.
Schlingmann KP, et al.
J Am Soc Nephrol. 2016 Feb;27(2):604-14. doi: 10.1681/ASN.2014101025. Epub 2015 Jun 5.
J Am Soc Nephrol. 2016.
PMID: 26047794
Free PMC article.
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