Hypotonia, Ataxia, and Delayed Development Syndrome caused by the EBF3 mutation in a Korean boy with muscle hypotonia
- Resource Type
- Article
- Source
- 대한의학유전학회지 17. 2 (2020): 92-96.
- Subject
Hypotonia Ataxia and Delayed Development Syndrome EBF3 Muscle hypotonia Developmental disabilities - Language
- Korean
- ISSN
- 12261769