(Q42589990)

3 November 2017

A specific superoxide dismutase mutation is on the same genetic background in sporadic and familial cases of amyotrophic lateral sclerosis (English)

1 reference

amyotrophic lateral sclerosis

3 November 2017

0 references

author name string

Hayward C

1

1 reference

3 November 2017

Swingler RJ

2

1 reference

3 November 2017

Simpson SA

3

1 reference

3 November 2017

Brock DJ

4

1 reference

3 November 2017

language of work or name

English

0 references

publication date

1 November 1996

1 reference

American Journal of Human Genetics

3 November 2017

1 reference

3 November 2017

59

1 reference

3 November 2017

5

1 reference

3 November 2017

1165-1167

1 reference

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

3 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914828

Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914828

Integration of gene maps: chromosome 21.

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914828

A powerful likelihood method for the analysis of linkage disequilibrium between trait loci and one or more polymorphic marker loci

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914828

Random search for shared chromosomal regions in four affected individuals: the assignment of a new hereditary ataxia locus

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914828

Superoxide dismutase mutations in an unselected cohort of Scottish amyotrophic lateral sclerosis patients

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914828

Identification of a novel SOD1 mutation in an apparently sporadic amyotrophic lateral sclerosis patient and the detection of Ile113Thr in three others

28 May 2018

1 reference

12 December 2020

Identification of a novel exon 4 SOD1 mutation in a sporadic amyotrophic lateral sclerosis patient

1 reference

12 December 2020

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

1 reference

12 December 2020

Familial adult motor neuron disease: amyotrophic lateral sclerosis

1 reference

12 December 2020

Cu/Zn superoxide dismutase (SOD1) mutations and sporadic amyotrophic lateral sclerosis

1 reference

12 December 2020

Two novel SOD1 mutations in patients with familial amyotrophic lateral sclerosis

1 reference

12 December 2020

Identifiers

1 reference

3 November 2017

PubMed publication ID

8900247

1 reference