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Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans

Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans

Details

Database :
OpenAIRE
Journal :
Europe PubMed Central
Accession number :
edsair.dedup.wf.001..4d6d39b7e920b7645fb4e80f3da03e84