Expanding the phenotypic spectrum of TRIT1 mutatins, a cause of severe autosomal recessive microcephalyT. Smol,P. Brunelle,O. Boute-Benejean, J. A. Basseti,M. Figeac,L. Faivre,F. Petit,C. Thauvin-Robinet,Q. Thomas,F. Tran-Mau-Them,S. Manouvrier-Hanu,J. GhoumidEUROPEAN JOURNAL OF HUMAN GENETICS(2019)引用 0|浏览31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