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Q27000375-09454532-4B2B-45A3-A890-36B0B3AEE2F2
Q27000375-09454532-4B2B-45A3-A890-36B0B3AEE2F2
BestRank
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http://www.wikidata.org/entity/statement/Q27000375-09454532-4B2B-45A3-A890-36B0B3AEE2F2
Lower urinary tract development and disease
P2860
Q27000375-09454532-4B2B-45A3-A890-36B0B3AEE2F2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q27000375-09454532-4B2B-45A3-A890-36B0B3AEE2F2
rank
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wasDerivedFrom
0ab40cb61011ae50c9c47abf815ecb5c79e1fcf8
P2860
HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort.