NR2F1 haploinsufficiency is associated with optic atrophy, dysmorphism and global developmental delay
Year: 2013
Type: article
DOI: 10.1002/ajmg.a.35650
Institution: Washington University in St. Louis
Language: English
Topic: Genomics and Rare Diseases
Subfield: Genetics
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2170967913
