Expanding Genotype–phenotype Correlations in FOXG1 Syndrome: Results from a Patient Registry
Orphanet Journal of Rare Diseases（2023）
关键词
Patient registry,Genotype–phenotype association,Rare neurological diseases,Movement Disorder,Epilepsy
AI 理解论文
溯源树
样例
生成溯源树，研究论文发展脉络
Chat Paper
正在生成论文摘要