(Q34156857)

31 July 2017

Senataxin mutations and amyotrophic lateral sclerosis (English)

1 reference

amyotrophic lateral sclerosis

31 July 2017

0 references

3

Hiroshi Mitsumoto

1 reference

31 July 2017

Michio Hirano

1

1 reference

31 July 2017

Catarina M Quinzii

2

1 reference

31 July 2017

Arthur P Hays

4

1 reference

31 July 2017

J Kirk Roberts

5

1 reference

31 July 2017

Patricia Richard

6

1 reference

31 July 2017

Lewis P Rowland

7

1 reference

31 July 2017

29 December 2010

1 reference

Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders

31 July 2017

1 reference

31 July 2017

12

1 reference

31 July 2017

3

1 reference

31 July 2017

223-227

1 reference

Molecular biology of amyotrophic lateral sclerosis: insights from genetics

31 July 2017

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2010.545952

Genetics of motor neuron disorders: new insights into pathogenic mechanisms

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2010.545952

Genetic studies of amyotrophic lateral sclerosis: controversies and perspectives

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2010.545952

Hereditary motor system diseases (chronic juvenile amyotrophic lateral sclerosis). Conditions combining a bilateral pyramidal syndrome with limb and bulbar amyotrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2010.545952

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2010.545952

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/10.3109%2F17482968.2010.545952

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2010.545952

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2010.545952

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/10.3109%2F17482968.2010.545952

Cerebellar ataxia with oculomotor apraxia type 1: clinical and genetic studies

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2010.545952

Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2010.545952

Identification and characterisation of a large senataxin (SETX) gene duplication in ataxia with ocular apraxia type 2 (AOA2).

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2010.545952

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2010.545952

Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic study.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2010.545952

Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype-phenotype correlation study.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2010.545952

Ataxia oculomotor apraxia type 2: course over 27 years and a novel stop mutation in the senataxin gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2010.545952

Senataxin, the yeast Sen1p orthologue: characterization of a unique protein in which recessive mutations cause ataxia and dominant mutations cause motor neuron disease

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2010.545952

NERVE CONDUCTION AND OTHER STUDIES IN FAMILIES WITH CHARCOT-MARIE-TOOTH DISEASE

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2010.545952

Autosomal dominant juvenile amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2010.545952

RNA processing defects associated with diseases of the motor neuron

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2010.545952

The basic aspects of therapeutics in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2010.545952

Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21190393

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Rate of familial amyotrophic lateral sclerosis: a systematic review and meta-analysis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21190393

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Research advances in amyotrophic lateral sclerosis, 2009 to 2010.

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21190393

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.3109/17482968.2010.545952

1 reference

31 July 2017

1 reference