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Q35670536-1FF2D3C4-F1B0-4215-96F5-D54D013BE071
Q35670536-1FF2D3C4-F1B0-4215-96F5-D54D013BE071
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35670536-1FF2D3C4-F1B0-4215-96F5-D54D013BE071
HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort.
P2860
Q35670536-1FF2D3C4-F1B0-4215-96F5-D54D013BE071
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35670536-1FF2D3C4-F1B0-4215-96F5-D54D013BE071
rank
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type
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Statement
wasDerivedFrom
21d562781a87c24ec10928bd7dc67a7afa058bb6
P2860
Clinical spectrum associated with hepatocyte nuclear factor-1beta mutations.