| 标题 |
Advanced iPSC-based modelling of LMNA-related congenital muscular dystrophy enables development of genetic therapies for muscle laminopathies |
| 网址 | |
| DOI | |
| 其它 |
期刊:Molecular therapy : the journal of the American Society of Gene Therapy 作者:Moore D; Steele-Stallard H; Pinton L; Lionello VM; Rossi L; et al 出版日期:2026/08/19 |
| 求助人 | |
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(2025-6-4)