(Q36165139)

12 August 2017

A novel exon 2 I27V VCP variant is associated with dissimilar clinical syndromes (English)

1 reference

12 August 2017

Jonathan D Rohrer

1

0 references

Jason D. Warren

object named as

Jason D Warren

2

0 references

Martin Rossor

object named as

Martin N Rossor

7

0 references

John Collinge

6

object named as

John Collinge

1 reference

12 August 2017

David Reiman

3

1 reference

12 August 2017

James Uphill

4

1 reference

12 August 2017

Jonathan Beck

5

1 reference

12 August 2017

Adrian M Isaacs

8

1 reference

12 August 2017

Simon Mead

9

1 reference

12 August 2017

language of work or name

1 reference

9 March 2011

1 reference

12 August 2017

1 reference

12 August 2017

258

1 reference

12 August 2017

8

1 reference

12 August 2017

1494-1496

1 reference

https://scigraph.springernature.com/pub.10.1007/s00415-011-5966-4

12 August 2017

0 references

cites work

Exome sequencing reveals VCP mutations as a cause of familial ALS

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606971

The heritability and genetics of frontotemporal lobar degeneration.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606971

Valosin-containing protein disease: inclusion body myopathy with Paget's disease of the bone and fronto-temporal dementia

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606971

Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606971

Valosin-containing protein and the pathogenesis of frontotemporal dementia associated with inclusion body myopathy

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606971

Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606971

TDP-43 pathology in familial frontotemporal dementia and motor neuron disease without Progranulin mutations

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606971

TDP-43 in the ubiquitin pathology of frontotemporal dementia with VCP gene mutations.

2 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606971

PSIC: profile extraction from sequence alignments with position-specific counts of independent observations.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606971

Novel ubiquitin neuropathology in frontotemporal dementia with valosin-containing protein gene mutations

23 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21387114

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S00415-011-5966-4

1 reference

12 August 2017

1 reference

12 August 2017

PubMed publication ID

21387114

1 reference