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

✍ Scribed by Shore, Eileen M; Xu, Meiqi; Feldman, George J; Fenstermacher, David A; Brown, Matthew A; Kaplan, Frederick S

No coin nor oath required. For personal study only.

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A recurrent mutation in the BMP type I r

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Classic and atypical fibrodysplasia ossi

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between some ACVR1 mutations and the age of onset of heterotopic ossification or on embryonic skeletal development.