Heterozygous loss-of-function DHX9 variants are associated with neurodevelopmental disorders: Human genetic and experimental evidences
- Resource Type
- Article
- Authors
- Yamada, Mamiko; Nitta, Yohei; Uehara, Tomoko; Suzuki, Hisato; Miya, Fuyuki; Takenouchi, Toshiki; Tamura, Masaru; Ayabe, Shinya; Yoshiki, Atsushi; Maeno, Akiteru; Saga, Yumiko; Furuse, Tamio; Yamada, Ikuko; Okamoto, Nobuhiko; Kosaki, Kenjiro; Sugie, Atsushi
- Source
- In European Journal of Medical Genetics August 2023 66(8)
- Subject
- Language
- ISSN
- 1769-7212