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Q35156029-5A7FFCB1-4597-4269-A64B-2EB9DD89E688
Q35156029-5A7FFCB1-4597-4269-A64B-2EB9DD89E688
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Statement
http://www.wikidata.org/entity/statement/Q35156029-5A7FFCB1-4597-4269-A64B-2EB9DD89E688
Long-term clinical outcome and carrier phenotype in autosomal recessive hypophosphatemia caused by a novel DMP1 mutation.
P2860
Q35156029-5A7FFCB1-4597-4269-A64B-2EB9DD89E688
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35156029-5A7FFCB1-4597-4269-A64B-2EB9DD89E688
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wasDerivedFrom
7ee4a7f15e0d97793389a93092deeab3a37d691e
P2860
Dmp1-deficient mice display severe defects in cartilage formation responsible for a chondrodysplasia-like phenotype