- Concurrent progress of reprogramming and gene correction to overcome therapeutic limitation of mutant ALK2-iPSC
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Kim BY, Jeong S, Lee SY, Lee SM, Gweon EJ, Ahn H, Kim J, Chung SK
- KMID: 2361524
- Exp Mol Med.
- 2016 Jun;48(6):e237.
- doi: 10.1038/emm.2016.43
Fibrodysplasia ossificans progressiva (FOP) syndrome is caused by mutation of the gene ACVR1, encoding a constitutive active bone morphogenetic protein type I receptor (also called ALK2) to induce heterotopic ossification... -
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