Novel FDXR pathogenic variants expand the clinical spectrum related to human ferredoxin reductase defectsD. Piekutowska-Abramczuk,S. L. Stenton,M. Gusic,E. Ciara,M. Wagner,T. Haack,K. G. Claeys, L. Schrod,C. Nava,V. Narayanan,D. Jurkiewicz, P. Halat-Wolska,M. Pelc,K. Chrzanowska,R. Ploski, T. Meitinger,M. Pronicki,E. Pronicka,H. ProkischEUROPEAN JOURNAL OF HUMAN GENETICS(2019)引用 0|浏览36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