Dominant negative heterozygous mutation in Erlin2 prevents degradation of IP3 receptors and is responsible for hereditary spastic paraplegia 37
EUROPEAN JOURNAL OF HUMAN GENETICS(2019)
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(2019)