Karen Stals

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Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays - European Journal of Human Genetics

Jul 27, 2023 | nature.com | Dong Li |Susan White |Julia Soares Baptista |Karen Stals |Benjamin Cogné |Angela Peron | +6 more

AbstractNuclear receptor subfamily 2 group F member 2 (NR2F2 or COUP-TF2) encodes a transcription factor which is expressed at high levels during mammalian development.

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