(Q45930181)

English

Inclusion body myopathy with Paget disease of the bone and frontotemporal dementia associated with a novel G156S mutation in the VCP gene.

scientific article published on 19 July 2013

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/23868359

Inclusion body myopathy with Paget disease of the bone and frontotemporal dementia associated with a novel G156S mutation in the VCP gene. (English)

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/23868359

frontotemporal dementia

1 reference

based on heuristic

inferred from title

author name string

Junji Komatsu

1

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/23868359

Kazuo Iwasa

2

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/23868359

Daisuke Yanase

3

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/23868359

Masahito Yamada

4

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/23868359

publication date

19 July 2013

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/23868359

Muscle and Nerve

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/23868359

Japanese version of the Frontal Assessment Battery for dementia

1 reference

https://api.crossref.org/works/10.1002%2FMUS.23960

21 January 2018

Exome sequencing reveals VCP mutations as a cause of familial ALS

1 reference

https://api.crossref.org/works/10.1002%2FMUS.23960

21 January 2018

The multiple faces of valosin-containing protein-associated diseases: inclusion body myopathy with Paget's disease of bone, frontotemporal dementia, and amyotrophic lateral sclerosis.

1 reference

https://api.crossref.org/works/10.1002%2FMUS.23960

21 January 2018

Pathological consequences of VCP mutations on human striated muscle.

1 reference

https://api.crossref.org/works/10.1002%2FMUS.23960

21 January 2018

A novel mutation in the VCP gene (G157R) in a German family with inclusion-body myopathy with Paget disease of bone and frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1002%2FMUS.23960

21 January 2018

Emerging functions of the VCP/p97 AAA-ATPase in the ubiquitin system

1 reference

https://api.crossref.org/works/10.1002%2FMUS.23960

21 January 2018

Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159His

1 reference

https://api.crossref.org/works/10.1002%2FMUS.23960

21 January 2018

Identifiers

10.1002/MUS.23960

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/23868359

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/23868359

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