Skip to content
VuFind
English
Deutsch
Español
Français
Italiano
日本語
Nederlands
Português
Português (Brasil)
中文(简体)
中文(繁體)
Türkçe
עברית
Gaeilge
Cymraeg
Ελληνικά
Català
Euskara
Русский
Čeština
Suomi
Svenska
polski
Dansk
slovenščina
اللغة العربية
বাংলা
Galego
Tiếng Việt
Hrvatski
हिंदी
Հայերէն
Українська
Sámegiella
Монгол
Language
All Fields
Title
Author
Subject
Call Number
ISBN/ISSN
Tag
Find
Advanced
Identification of a novel muta...
Cite this
Text this
Email this
Print
Export Record
Export to RefWorks
Export to EndNoteWeb
Export to EndNote
Permanent link
Identification of a novel mutation in activin receptor type 1 (ACVR1) in a fibrodysplasia ossificans progressiva (FOP) patient
Bibliographic Details
Main Authors:
Petrie, K
,
Pointon, J
,
Atukorala, I
,
Russell, R
,
Wordsworth, P
,
Triffitt, J
Format:
Journal article
Published:
2007
Holdings
Description
Similar Items
Staff View
Description
Summary:
Similar Items
An atypical mutation in the activin a receptor, type 1 gene (ACVR1) in a severely affected Fibrodysplasia Ossificans Progressiva patient
by: Petrie, K, et al.
Published: (2007)
Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients.
by: Petrie, K, et al.
Published: (2009)
Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients.
by: Petrie, K, et al.
Published: (2009)
Anti-ACVR1 antibodies exacerbate heterotopic ossification in fibrodysplasia ossificans progressiva (FOP) by activating FOP-mutant ACVR1
by: Senem Aykul, et al.
Published: (2022-06-01)
ACVR1 mutation and Fibrodysplasia Ossificans Progressiva in Chinese children
by: Ng Bobby KW, et al.
Published: (2011-09-01)