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

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APA Style

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., & Kaplan, F. (2007). Erratum: 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.

MLA Style

Shore, E., et al. “Erratum: 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, vol. 39, no. 2, 2007, pp. 276–76.

Chicago Style

Shore, E, M Xu, G Feldman, D Fenstermacher, T Cho, I Choi, J Connor, et al. 2007. “Erratum: 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): 276–76.
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Publisher copy:: 10.1038/ng0207-276b

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+ Xu, M More by this author

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+ Feldman, G More by this author

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+ Fenstermacher, D More by this author

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+ Cho, T More by this author

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Bibliographic Details

Journal:: Nature Genetics
Volume:: 39
Issue:: 2
Pages:: 276-276
Publication date:: 2007-02-01
DOI:: 10.1038/ng0207-276b
EISSN:: 1546-1718
ISSN:: 1061-4036

Item Description

Language:: English
Pubs id:: pubs:109650
UUID:: uuid:c568122a-3920-4b0b-8795-a96043e2d189
Local pid:: pubs:109650
Source identifiers:: 109650
Deposit date:: 2014-02-10

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Copyright date:: 2007

Licence:: Terms and Conditions of Use for Oxford University Research Archive

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