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Q38731983-F27479F6-E01A-47FB-A19C-673081B9FF52
Q38731983-F27479F6-E01A-47FB-A19C-673081B9FF52
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Statement
http://www.wikidata.org/entity/statement/Q38731983-F27479F6-E01A-47FB-A19C-673081B9FF52
Genetics of Congenital Anomalies of the Kidney and Urinary Tract: The Current State of Play.
P2860
Q38731983-F27479F6-E01A-47FB-A19C-673081B9FF52
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38731983-F27479F6-E01A-47FB-A19C-673081B9FF52
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wasDerivedFrom
16e238976209fb7fbd59041160336b18c32bd086
P2860
HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort.