Identification of a new mutation confirms the implication of IFT27 in Bardet-Biedl Syndrome (BBS19)E. Schaefer,C. Stoetzel,V. Geoffroy,L. Mary,C. Marks,M. Holder, J. Ghoumid,H. Dollfus,J. MullerEUROPEAN JOURNAL OF HUMAN GENETICS(2019)引用 0|浏览19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