학술논문
Recurrent FOXP4 nonsense variant in two unrelated patients: Association with neurodevelopmental disease and congenital diaphragmatic hernia
Document Type
Article
Author
Source
In: American Journal of Medical Genetics, Part A . (American Journal of Medical Genetics, Part A, January 2023, 191(1):259-264)
Subject
Language
English
ISSN
15524833
15524825
15524825