De novo heterozygous HSPD1 variants: A novel mechanism in hypomyelinating leukodystrophy type 4? L. Brick,P. Bross,D. Ang, C. Comert,J. Palmfeldt, B. F. Meaney, M. Kozenko,C. GeorgopoulosEUROPEAN JOURNAL OF HUMAN GENETICS（2019）引用 0|浏览4暂无评分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
