A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva-Reference-Cited by-同舟云学术

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

Published:2006-04-23 Issue:5 Volume:38 Page:525-527
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Shore Eileen M,Xu Meiqi,Feldman George J,Fenstermacher David A,Cho Tae-Joon,Choi In Ho,Connor J Michael,Delai Patricia,Glaser David L,LeMerrer Martine,Morhart Rolf,Rogers John G,Smith Roger,Triffitt James T,Urtizberea J Andoni,Zasloff Michael,Brown Matthew A,Kaplan Frederick S

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1783.pdf

Reference15 articles.

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2. Shore, E.M. et al. Clin. Rev. Bone Miner. Metab. 3, 201–204 (2005).

3. Feldman, G. et al. Am. J. Hum. Genet. 66, 128–135 (2000).

4. Attisano, L. et al. Cell 75, 671–680 (1993).

5. Payne, T.L. et al. Mech. Dev. 100, 275–289 (2001).

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