(Q52917234)

9 May 2018

title

Heterozygous S44L missense change of the spastin gene in amyotrophic lateral sclerosis. (English)

1 reference

9 May 2018

amyotrophic lateral sclerosis

main subject

0 references

1 reference

Christoph Münch

1

1 reference

9 May 2018

Arndt Rolfs

series ordinal

2

1 reference

9 May 2018

Thomas Meyer

series ordinal

3

1 reference

9 May 2018

publication date

1 August 2008

1 reference

9 May 2018

Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders

published in

1 reference

9 May 2018

volume

9

1 reference

9 May 2018

issue

4

1 reference

9 May 2018

page(s)

251-253

1 reference

9 May 2018

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

cites work

1 reference

https://api.crossref.org/works/10.1080%2F17482960801900172

The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960801900172

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%2F17482960801900172

A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960801900172

Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960801900172

The hereditary spastic paraplegias: nine genes and counting

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960801900172

Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960801900172

Early-onset ALS with long-term survival associated with spastin gene mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960801900172

The cellular and molecular pathology of the motor system in hereditary spastic paraparesis due to mutation of the spastin gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960801900172

Intragenic modifiers of hereditary spastic paraplegia due to spastin gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960801900172

Spastin mutations are frequent in sporadic spastic paraparesis and their spectrum is different from that observed in familial cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960801900172

Mutation analysis of the spastin gene (SPG4) in patients with hereditary spastic paraparesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960801900172

Spastin mutations in sporadic adult-onset upper motor neuron syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17482960801900172

10.1080/17482960801900172

21 January 2018

Identifiers

DOI

1 reference

9 May 2018

1 reference

9 May 2018