An atypical mutation in the activin a receptor, type 1 gene (ACVR1) in a severely affected Fibrodysplasia Ossificans Progressiva patient
Autors principals: | Petrie, K, Pointon, J, Smith, R, Russell, R, Wordsworth, P, Triffitt, J |
---|---|
Format: | Conference item |
Publicat: |
2007
|
Ítems similars
-
Identification of a novel mutation in activin receptor type 1 (ACVR1) in a fibrodysplasia ossificans progressiva (FOP) patient
per: Petrie, K, et al.
Publicat: (2007) -
Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients.
per: Petrie, K, et al.
Publicat: (2009) -
Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients.
per: Petrie, K, et al.
Publicat: (2009) -
ACVR1 mutation and Fibrodysplasia Ossificans Progressiva in Chinese children
per: Ng Bobby KW, et al.
Publicat: (2011-09-01) -
Mutation Detection in Activin A Receptor, Type I (ACVR1) Gene in Fibrodysplasia Ossificans Progressiva in An Iranian Family
per: Ziba Morovvati, et al.
Publicat: (2014-03-01)