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Q48312233-43CC984F-B7FA-4AE5-87F1-0CCEBC9A6E78
Q48312233-43CC984F-B7FA-4AE5-87F1-0CCEBC9A6E78
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http://www.wikidata.org/entity/statement/Q48312233-43CC984F-B7FA-4AE5-87F1-0CCEBC9A6E78
Mutational analysis of PHEX, FGF23 and CLCN5 in patients with hypophosphataemic rickets.
P2860
Q48312233-43CC984F-B7FA-4AE5-87F1-0CCEBC9A6E78
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48312233-43CC984F-B7FA-4AE5-87F1-0CCEBC9A6E78
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wasDerivedFrom
deaf5394552a19895c581216f2ead36e2985962d
P2860
An autosomal dominant hypophosphatemic rickets phenotype in a Tunisian family caused by a new FGF23 missense mutation.