(Q38074000)

28 August 2017

1 reference

title

Motor neuron disease in 2012: Novel causal genes and disease modifiers (English)

1 reference

28 August 2017

1 reference

Marka van Blitterswijk

series ordinal

2

object named as

Marka van Blitterswijk

0 references

Rosa Rademakers

series ordinal

1

object named as

Rosa Rademakers

1 reference

PubMed ID

23318296

28 August 2017

language of work or name

English

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publication date

15 January 2013

1 reference

28 August 2017

Nature Reviews Neurology

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28 August 2017

9

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28 August 2017

2

1 reference

28 August 2017

63-64

1 reference

https://scigraph.springernature.com/pub.10.1038/nrneurol.2012.276

28 August 2017

0 references

cites work

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2012.276

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2012.276

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2012.276

How do C9ORF72 repeat expansions cause amyotrophic lateral sclerosis and frontotemporal dementia: can we learn from other noncoding repeat expansion disorders?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2012.276

Amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2012.276

Familial frontotemporal dementia and amyotrophic lateral sclerosis associated with the C9ORF72 hexanucleotide repeat.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2012.276

Evidence for an oligogenic basis of amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2012.276

Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2012.276

EPHA4 is a disease modifier of amyotrophic lateral sclerosis in animal models and in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2012.276

Inhibition of RNA lariat debranching enzyme suppresses TDP-43 toxicity in ALS disease models

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2012.276

10.1038/NRNEUROL.2012.276

21 January 2018

Identifiers

DOI

1 reference

PubMed ID

23318296

Dimensions Publication ID

28 August 2017

0 references

1 reference

PubMed ID

23318296