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

Bibliographic Details
Main Authors: 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
Format: Journal article
Language:English
Published: 2007
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author 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
author_facet 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
author_sort Shore, E
collection OXFORD
description
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institution University of Oxford
language English
last_indexed 2024-03-07T04:03:34Z
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spelling oxford-uuid:c568122a-3920-4b0b-8795-a96043e2d1892022-03-27T06:30:36ZErratum: A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva (Nature Genetics (2006) 38, (525-527))Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:c568122a-3920-4b0b-8795-a96043e2d189EnglishSymplectic Elements at Oxford2007Shore, EXu, MFeldman, GFenstermacher, DCho, TChoi, IConnor, JDelai, PGlaser, DLeMerrer, MMorhart, RRogers, JSmith, RTriffitt, JUrtizberea, JZasloff, MBrown, MKaplan, F
spellingShingle 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
Erratum: A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva (Nature Genetics (2006) 38, (525-527))
title Erratum: A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva (Nature Genetics (2006) 38, (525-527))
title_full Erratum: A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva (Nature Genetics (2006) 38, (525-527))
title_fullStr Erratum: A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva (Nature Genetics (2006) 38, (525-527))
title_full_unstemmed Erratum: A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva (Nature Genetics (2006) 38, (525-527))
title_short Erratum: A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva (Nature Genetics (2006) 38, (525-527))
title_sort 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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