(Q41732013)

8 October 2017

Gigaxonin mutation analysis in patients with NIFID. (English)

1 reference

8 October 2017

2

Nigel J Cairns

1 reference

8 October 2017

4

Jean-Pierre Julien

1 reference

8 October 2017

3

Eileen H Bigio

1 reference

8 October 2017

Florence Dequen

1

1 reference

PMCID

2987523

8 October 2017

language of work or name

1 reference

26 September 2009

1 reference

8 October 2017

Neurobiology of Aging

1 reference

8 October 2017

32

1 reference

8 October 2017

8

1 reference

8 October 2017

1528-1529

1 reference

Modest loss of peripheral axons, muscle atrophy and formation of brain inclusions in mice with targeted deletion of gigaxonin exon 1

8 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987523

alpha-Internexin aggregates are abundant in neuronal intermediate filament inclusion disease (NIFID) but rare in other neurodegenerative diseases

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987523

Giant axonal neuropathy (GAN): case report and two novel mutations in the gigaxonin gene

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987523

The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987523

Mutation analysis of patients with neuronal intermediate filament inclusion disease (NIFID).

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987523

10.1016/J.NEUROBIOLAGING.2009.08.018

18 August 2018

Identifiers

DOI

1 reference

8 October 2017

1 reference

8 October 2017

1 reference

PMCID

2987523