Chrome Extension
WeChat Mini Program
Use on ChatGLM

U2AF2 Variant in a Patient with Developmental Delay, Dysmorphic Features, and Epilepsy.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A(2023)

Cited 1|Views7
Key words
developmental delay,epilepsy,missense variant,neurodevelopment,RNA binding protein,U2AF2
AI Read Science
Must-Reading Tree
Example
Generate MRT to find the research sequence of this paper
Chat Paper
Summary is being generated by the instructions you defined