G.O.4: The SMCHD1 mutation spectrum in FSHD2: Novel insight in clinical variability in FSHD T.L. van den Boogaard, R.J.L. Lemmers, P. Camano,P.J. van der Vliet, J. Balog, N. Voermans, S.J. Tapscott, A.L. de Munain, R. Tawil, B. Bakker, S.M. MaarelNeuromuscular Disorders（2014）引用 0|浏览0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
