A novel GNAO1 mutation in a patient with severe movement disorderD. Piekutowska-Abramczuk,H. Mierzewska,E. Ciara,J. Trubicka,D. Jurkiewicz,D. Rokicki,A. Jacoszek,M. Pronicki,P. Stawinski, P. Halat,M. Pelc, J. Ksiazyk,M. Krajewska-Walasek,R. Ploski,E. PronickaEUROPEAN JOURNAL OF HUMAN GENETICS(2018)引用 0|浏览25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