An atypical mutation in the activin a receptor, type 1 gene (ACVR1) in a severely affected Fibrodysplasia Ossificans Progressiva patient

Detalles Bibliográficos
Autores principales:	Petrie, K, Pointon, J, Smith, R, Russell, R, Wordsworth, P, Triffitt, J
Formato:	Conference item
Publicado:	2007

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