A recurrent mutation in IER3IP1 causing microcephaly with simplified gyral pattern, epilepsy and permanent neonatal diabetes syndrome (MEDS)
EUROPEAN JOURNAL OF HUMAN GENETICS(2018)
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
EUROPEAN JOURNAL OF HUMAN GENETICS(2018)