N.P.3 02 Wide clinical spectrum of CMT4C disease in patients homozygous for the p.Arg1109X mutation in SH3TC2 geneJ. Colomer,R. Gooding,D. Angelicheva,R.H.M. King,Y. Parman,A. Nascimento,J. Conill,L. KalaydjievaNeuromuscular Disorders(2006)引用 0|浏览8暂无评分关键词spectrumAI 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