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1
Q47904747-1CC32F9F-CFCD-444F-9453-7E0268301892
Q47904747-1CC32F9F-CFCD-444F-9453-7E0268301892
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http://www.wikidata.org/entity/statement/Q47904747-1CC32F9F-CFCD-444F-9453-7E0268301892
Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesis.
P2860
Q47904747-1CC32F9F-CFCD-444F-9453-7E0268301892
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47904747-1CC32F9F-CFCD-444F-9453-7E0268301892
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wasDerivedFrom
e231940d08cd3b3627f202d531034d9d8402d70b
P2860
Transcription factor gene MNX1 is a novel cause of permanent neonatal diabetes in a consanguineous family.