✦ LIBER ✦

A novel mutation of ALK2, L196P, found in the most benign case of fibrodysplasia ossificans progressiva activates BMP-specific intracellular signaling equivalent to a typical mutation, R206H

✍ Scribed by Satoshi Ohte; Masashi Shin; Hiroki Sasanuma; Katsumi Yoneyama; Masumi Akita; Kenji Ikebuchi; Eijiro Jimi; Yuichi Maruki; Masaru Matsuoka; Akira Namba; Hiroshi Tomoda; Yasushi Okazaki; Akira Ohtake; Hiromi Oda; Ichiro Owan; Tetsuya Yoda; Hirokazu Furuya; Jyunji Kamizono; Hiroshi Kitoh; Yasuharu Nakashima; Takafumi Susami; Nobuhiko Haga; Tetsuo Komori; Takenobu Katagiri

Book ID: 116301529
Publisher: Elsevier Science
Year: 2011
Tongue: English
Weight: 457 KB
Volume: 407
Category: Article
ISSN: 0006-291X
DOI: 10.1016/j.bbrc.2011.03.001

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A novel mutation ACVR1 in the glycine/se

A novel mutation ACVR1 in the glycine/serine-rich domain found in the most benign case of fibrodysplasia ossificans progressiva reported to date

✍ C. Gregson⁎; P. Hollingworth; M. Williams; K. Petrie; A. Bullock; J. Tobias; J. 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 73 KB

A novel ACVR1 mutation in the glycine/se

A novel ACVR1 mutation in the glycine/serine-rich domain found in the most benign case of a fibrodysplasia ossificans progressiva variant reported to date

✍ Celia L. Gregson; Peter Hollingworth; Martin Williams; Kirsten A. Petrie; Alex N 📂 Article 📅 2011 🏛 Elsevier Science 🌐 English ⚖ 651 KB