G.P.12.07 A new ACTA1 mutation in two unrelated sporadic cases of neonatal form of CFTDN. Deconinck,N. Monnier,M.C. Commare,P. Mezin,A. Michotte,J. LunardiNEUROMUSCULAR DISORDERS(2009)引用 0|浏览9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