(Q37232034)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19543505%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

title

ACVR1 gene mutation in sporadic Korean patients with fibrodysplasia ossificans progressiva (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19543505%20AND%20SRC:MED&resulttype=core&format=json

fibrodysplasia ossificans progressiva

1 February 2020

main subject

0 references

author

Tae-Joon Cho

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19543505%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

author name string

Dong Yeon Lee

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19543505%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

Hye Ran Lee

3

1 reference

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1 February 2020

Moon Seok Park

4

1 reference

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1 February 2020

Won Joon Yoo

5

1 reference

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1 February 2020

Chin Youb Chung

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19543505%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

In Ho Choi

7

1 reference

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1 February 2020

publication date

12 June 2009

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19543505%20AND%20SRC:MED&resulttype=core&format=json

Journal of Korean Medical Science

1 February 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19543505%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

volume

24

1 reference

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1 February 2020

issue

3

1 reference

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1 February 2020

page(s)

433-437

1 reference

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Creative Commons Attribution-NonCommercial 3.0 Unported

1 February 2020

copyright license

start time

1 January 2009

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2698188

The origins, patterns and implications of human spontaneous mutation

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2698188

Iatrogenic harm caused by diagnostic errors in fibrodysplasia ossificans progressiva

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2698188

Fibrodysplasia ossificans progressiva. The clinical features and natural history of 34 patients.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2698188

The natural history of heterotopic ossification in patients who have fibrodysplasia ossificans progressiva. A study of forty-four patients

3 September 2018

1 reference

12 December 2020

The histopathology of fibrodysplasia ossificans progressiva. An endochondral process

1 reference

12 December 2020

Mild expression of fibrodysplasia ossificans progressiva: a report of 3 cases

1 reference

12 December 2020

Fibrodysplasia ossificans progressiva (FOP)

1 reference

12 December 2020

De novo 617G-A nucleotide mutation in the ACVR1 gene in a Taiwanese patient with fibrodysplasia ossificans progressiva

1 reference

12 December 2020

The ACVR1 617G>A mutation is also recurrent in three Japanese patients with fibrodysplasia ossificans progressiva

1 reference

12 December 2020

Functional modeling of the ACVR1 (R206H) mutation in FOP

1 reference

12 December 2020

10.3346/JKMS.2009.24.3.433

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19543505%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

1 reference

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1 February 2020

PubMed publication ID

19543505

1 reference