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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

✍ Scribed by J.K. Köhle; K. Kapelari; D. Kotzot; T.M. Strom; L.B. Zimmerhackl; W. Högler

Book ID
116322345
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
153 KB
Volume
45
Category
Article
ISSN
8756-3282

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