(Q54590330)

1 June 2018

title

Late-onset variant fibrodysplasia ossificans progressiva leading to misdiagnosis of ankylosing spondylitis. (English)

1 reference

1 June 2018

fibrodysplasia ossificans progressiva

main subject

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1 reference

Christopher P Barnett

series ordinal

1

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1 June 2018

Manish Dugar

series ordinal

2

1 reference

1 June 2018

Eric A Haan

series ordinal

3

1 reference

1 June 2018

language of work or name

English

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publication date

12 May 2011

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1 June 2018

American Journal of Medical Genetics

published in

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1 June 2018

volume

155A

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1 June 2018

issue

6

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1 June 2018

page(s)

1492-1495

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1 June 2018

Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.34003

Severe restriction in jaw movement after routine injection of local anesthetic in patients who have fibrodysplasia ossificans progressiva.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.34003

Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.34003

Insights from a rare genetic disorder of extra-skeletal bone formation, fibrodysplasia ossificans progressiva (FOP)

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.34003

A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.34003

21 January 2018

Identifiers

DOI

10.1002/AJMG.A.34003

1 reference

1 June 2018

1 reference

1 June 2018