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Hyperaminoaciduria and resolving phosphaturia in a family with autosomal dominant hypophosphataemic rickets (ADHR) due to a mutation in the FGF23 gene
J.K. Köhle, K. Kapelari, D. Kotzot, T.M. Strom, L.B. Zimmerhackl, W. HöglerVolume:
45
Year:
2009
Language:
english
Pages:
1
DOI:
10.1016/j.bone.2009.04.141
File:
PDF, 153 KB
english, 2009