A familial optic atrophy associated with mild neurodevelopmental disorder caused by SOX5 haploinsufficiency A. Gouronc, Y. Perdomo, L. Maurin, A. Schalk,S. El Chehadeh,E. Schaefer,H. Dollfus,S. ScheideckerEUROPEAN JOURNAL OF HUMAN GENETICS(2019)引用 0|浏览16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