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Q52673977-A684BF27-5484-4AF3-A076-8FCA030BE002
Q52673977-A684BF27-5484-4AF3-A076-8FCA030BE002
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http://www.wikidata.org/entity/statement/Q52673977-A684BF27-5484-4AF3-A076-8FCA030BE002
Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3.
P2860
Q52673977-A684BF27-5484-4AF3-A076-8FCA030BE002
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52673977-A684BF27-5484-4AF3-A076-8FCA030BE002
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wasDerivedFrom
9c2fa87287a6973a272e7316008b2bc5ecc43b6d
P2860
Genetic diagnosis of X-linked dominant Hypophosphatemic Rickets in a cohort study: tubular reabsorption of phosphate and 1,25(OH)2D serum levels are associated with PHEX mutation type.