FGF23 and Syndromes of Abnormal Renal Phosphate Handling-Reference-Cited by-同舟云学术

FGF23 and Syndromes of Abnormal Renal Phosphate Handling

Published:2012 Issue: Volume: Page:41-64
ISSN:0065-2598
Container-title:Advances in Experimental Medicine and Biology
language:
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Author:

Bergwitz Clemens,Jüppner Harald

Publisher

Springer US

Link

http://link.springer.com/content/pdf/10.1007/978-1-4614-0887-1_3.pdf

Reference172 articles.

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3. Econs M, McEnery P, Lennon F et al. Autosomal dominant hypophosphatemic rickets is linked to chromosome 12p13. J Clin Invest 1997; 100:2653–2657.

4. ADHR Consortium T. White KE, Evans WE et al. Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23. Nat Genet 2000; 26:345–348.

5. Gribaa M, Younes M, Bouyacoub Y et al. An autosomal dominant hypophosphatemic rickets phenotype in a Tunisian family caused by a new FGF23 missense mutation. J Bone Miner Metab 2009; 28:111–115.

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