Modification of CMT1 phenotypes by the independent coexisting neurogenetic disorders, McArdle disease and chromosome 5p trisomy.F P Thomas, T J Geller,A F Hahn, L Gutmann,X L Huang, H Wu,H E Wyandt, R V LeboAnnals of the New York Academy of Sciences（1999）引用 3|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
