Loss of function mutations in TCF12 cause autosomal dominant Kallmann syndrome and reveal network-level interactions between causal lociE. E. Davis,R. Balasubramanian, Z. A. Kupchinsky,D. Keefe,L. Plummer,B. Meczekalski,K. E. Heath, V. Lopez-Gonzalez, M. J. Ballesta-Martinez, G. Margabanthu, S. Price,J. Greening,M. E. Wierman,W. F. Crowley, N. KatsanisEUROPEAN JOURNAL OF HUMAN GENETICS（2019）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
