A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva (Nature Genetics (2006) 38, (525-527))

Shore, Eileen M., Xu, Meiqi, Feldman, George J., Fenstermacher, David A., Brown, Matthew A., Kaplan, Frederick S. and FOP Int Res Consortium (2007) A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva (Nature Genetics (2006) 38, (525-527)). Nature Genetics, 39 2: 276-276. doi:10.1038/ng0207-276b


Author Shore, Eileen M.
Xu, Meiqi
Feldman, George J.
Fenstermacher, David A.
Brown, Matthew A.
Kaplan, Frederick S.
FOP Int Res Consortium
Title A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva (Nature Genetics (2006) 38, (525-527))
Journal name Nature Genetics   Check publisher's open access policy
ISSN 1061-4036
1546-1718
Publication date 2007-02
Sub-type Correction/erratum
DOI 10.1038/ng0207-276b
Volume 39
Issue 2
Start page 276
End page 276
Total pages 1
Place of publication New York, NY, United States
Publisher Nature Publishing Group
Language eng
Q-Index Code CX
Q-Index Status Provisional Code
Institutional Status Unknown

Document type: Journal Article
Sub-type: Correction/erratum
Collection: School of Medicine Publications
 
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