Chrome Extension
WeChat Mini Program
Use on ChatGLM

Case Report: New Presentation of CLIFAHDD Syndrome with a Novel Variant in the NALCN Gene and a Literature Review

Yi Chen, Xiaotong Xia, Yiwen Zhang, Li Gao, Chenyiyi He,Jianguo Cao

FRONTIERS IN PEDIATRICS(2024)

Cited 0|Views6
Key words
CLIFAHDD syndrome,NALCN gene,missense variant,hypotonia,developmental delay,genetic testing
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