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

Detaylı Bibliyografya
Asıl Yazarlar: Petrie, K, Pointon, J, Smith, R, Russell, R, Wordsworth, P, Triffitt, J
Materyal Türü: Conference item
Baskı/Yayın Bilgisi: 2007