Shore, E. et al. (2006) A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva. Nature Genetics, 38(5), pp. 525-527. (doi: 10.1038/ng1783)
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| Item Type: | Articles |
|---|---|
| Status: | Published |
| Refereed: | Yes |
| Glasgow Author(s) Enlighten ID: | Connor, Prof J |
| Authors: | Shore, E., Xu, M., Feldman, G., Fenstermacher, D., Cho, T., Choi, I., Connor, J., Delai, P., Glaser, D., LeMerrer, M., Morhart, R., Rogers, J., Smith, R., Triffitt, J., Urtizberea, J., Zasloff, M., Brown, M., and Kaplan, F. |
| College/School: | College of Medical Veterinary and Life Sciences > School of Medicine, Dentistry & Nursing > Clinical Specialities |
| Journal Name: | Nature Genetics |
| ISSN: | 1061-4036 |
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