✦ LIBER ✦

A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva

✍ Scribed by Shore, Eileen M; Xu, Meiqi; Feldman, George J; Fenstermacher, David A; Brown, Matthew A; Kaplan, Frederick S

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Corrigendum: A recurrent mutation in the

✍ Shore, Eileen M; Xu, Meiqi; Feldman, George J; Fenstermacher, David A; Brown, Ma 📂 Article 📅 2007 🏛 Nature Publishing Group 🌐 English ⚖ 78 KB

Classic and atypical fibrodysplasia ossi

✍ Frederick S. Kaplan; Meiqi Xu; Petra Seemann; J. Michael Connor; David L. Glaser 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 496 KB

between some ACVR1 mutations and the age of onset of heterotopic ossification or on embryonic skeletal development.