An atypical mutation in the activin a receptor, type 1 gene (ACVR1) in a severely affected Fibrodysplasia Ossificans Progressiva patient
Үндсэн зохиолчид: | Petrie, K, Pointon, J, Smith, R, Russell, R, Wordsworth, P, Triffitt, J |
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Формат: | Conference item |
Хэвлэсэн: |
2007
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Ижил төстэй зүйлс
Ижил төстэй зүйлс
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Identification of a novel mutation in activin receptor type 1 (ACVR1) in a fibrodysplasia ossificans progressiva (FOP) patient
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Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients.
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Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients.
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Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients.
-н: Kirsten A Petrie, зэрэг
Хэвлэсэн: (2009-01-01) -
ACVR1 mutation and Fibrodysplasia Ossificans Progressiva in Chinese children
-н: Ng Bobby KW, зэрэг
Хэвлэсэн: (2011-09-01)