(Q54262060)

26 May 2018

title

A novel mutation in the senataxin gene identified in a Chinese patient with sporadic amyotrophic lateral sclerosis. (English)

1 reference

26 May 2018

amyotrophic lateral sclerosis

main subject

0 references

1 reference

Zhen-hua Zhao

1

1 reference

26 May 2018

Wen-Zu Chen

2

1 reference

26 May 2018

Zhi-ying Wu

3

1 reference

26 May 2018

Ning Wang

4

1 reference

26 May 2018

Gui-xian Zhao

5

1 reference

26 May 2018

Wan-jin Chen

6

1 reference

26 May 2018

Shen-xing Murong

7

1 reference

26 May 2018

publication date

1 April 2009

1 reference

26 May 2018

Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders

published in

1 reference

26 May 2018

volume

10

1 reference

26 May 2018

issue

2

1 reference

26 May 2018

page(s)

118-122

1 reference

26 May 2018

Amyotrophic lateral sclerosis.

cites work

1 reference

https://api.crossref.org/works/10.1080%2F17482960802572673

Molecular and cellular pathways of neurodegeneration in motor neurone disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960802572673

Prognosis in amyotrophic lateral sclerosis: a population-based study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960802572673

Molecular biology of amyotrophic lateral sclerosis: insights from genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960802572673

Genetics of familial and sporadic amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960802572673

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960802572673

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960802572673

TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960802572673

Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960802572673

DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4)

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960802572673

Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960802572673

Mutations in senataxin responsible for Quebec cluster of ataxia with neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960802572673

Autosomal recessive ataxia with peripheral neuropathy and elevated AFP: novel mutations in SETX.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960802572673

In cis autosomal dominant mutation of Senataxin associated with tremor/ataxia syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960802572673

Autosomal dominant juvenile amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960802572673

10.1080/17482960802572673

21 January 2018

Identifiers

DOI

1 reference

26 May 2018

PubMed ID

19058054

1 reference

26 May 2018