(Q48207820)

9 February 2018

title

Characterization of a novel SPG3A deletion in a French-Canadian family. (English)

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9 February 2018

14

Guy A Rouleau

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9 February 2018

5

Bernard Brais

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Nicolas Dupré

4

object named as

Nicolas Dupré

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9 February 2018

3

Sandra Laurent

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9 February 2018

Annie Levert

6

object named as

Annie Levert

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9 February 2018

author name string

Inge A Meijer

1

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9 February 2018

Patrick Dion

2

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9 February 2018

Jacques Puymirat

7

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9 February 2018

Marie France Rioux

8

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9 February 2018

Michel Sylvain

9

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9 February 2018

Peng-Peng Zhu

10

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9 February 2018

Cynthia Soderblom

11

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9 February 2018

Julia Stadler

12

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9 February 2018

Craig Blackstone

13

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9 February 2018

language of work or name

English

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publication date

1 June 2007

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9 February 2018

published in

Annals of Neurology

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9 February 2018

volume

61

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9 February 2018

page(s)

599-603

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9 February 2018

issue

6

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9 February 2018

Hereditary spastic paraplegias

cites work

1 reference

Autosomal recessive spastic paraplegia (SPG30) with mild ataxia and sensory neuropathy maps to chromosome 2q37.3.

21 January 2018

1 reference

Traffic accidents: molecular genetic insights into the pathogenesis of the hereditary spastic paraplegias

21 January 2018

1 reference

Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia

21 January 2018

1 reference

Further evidence that SPG3A gene mutations cause autosomal dominant hereditary spastic paraplegia

21 January 2018

1 reference

Novel mutations in the Atlastin gene (SPG3A) in families with autosomal dominant hereditary spastic paraplegia and evidence for late onset forms of HSP linked to the SPG3A locus

21 January 2018

1 reference

Novel mutation in the SPG3A gene in an African American family with an early onset of hereditary spastic paraplegia

21 January 2018

1 reference

Atlastin1 mutations are frequent in young-onset autosomal dominant spastic paraplegia

21 January 2018

1 reference

Incomplete penetrance in an SPG3A-linked family with a new mutation in the atlastin gene

21 January 2018

1 reference

Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A

21 January 2018

1 reference

The R495W mutation in SPG3A causes spastic paraplegia associated with axonal neuropathy.

21 January 2018

1 reference

SPG3A: An additional family carrying a new atlastin mutation

21 January 2018

1 reference

Cellular Localization, Oligomerization, and Membrane Association of the Hereditary Spastic Paraplegia 3A (SPG3A) Protein Atlastin

21 January 2018

1 reference

SPG3A protein atlastin-1 is enriched in growth cones and promotes axon elongation during neuronal development

21 January 2018

1 reference

Spastin and atlastin, two proteins mutated in autosomal-dominant hereditary spastic paraplegia, are binding partners

21 January 2018

1 reference

Interaction of two hereditary spastic paraplegia gene products, spastin and atlastin, suggests a common pathway for axonal maintenance

21 January 2018

1 reference

SPG3A mutation screening in English families with early onset autosomal dominant hereditary spastic paraplegia

21 January 2018

1 reference

A new locus for dominant hereditary spastic paraplegia maps to chromosome 2p12

21 January 2018

1 reference

Rapid Detection of CYP1A1, CYP2D6, and NAT Variants by Multiplex Polymerase Chain Reaction and Allele-Specific Oligonucleotide Assay

21 January 2018

1 reference

SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/ANA.21114

1 reference

9 February 2018

PubMed ID

17427918

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9 February 2018