Author response for "Variants in <i>NGLY1</i> lead to intellectual disability, myoclonus epilepsy, sensorimotor axonal polyneuropathy and mitochondrial dysfunction" Daan M. Panneman, Saskia B. Wortmann, Charlotte A. Haaxma, Peter M. Hasselt, Nicole I. Wolf, Yvonne Hendriks, Benno Küsters, Sjenet Emst‐de Vries, Els Westerlo, Werner J.H. Koopman, Liesbeth Wintjes, Frans Brandt, Maaike Vries, Dirk J. Lefeber, Jan A.M. Smeitink, Richard J. Rodenburgcrossref（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
