(Q47396282)

15 January 2018

title

Writer's cramp in an Australian pedigree with DYT1 dystonia (English)

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15 January 2018

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Mehdi van den Bos

1

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15 January 2018

Rosetta Marotta

2

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15 January 2018

Sandra Goldup

3

1 reference

15 January 2018

Tim Chataway

4

1 reference

15 January 2018

Frank Firgaira

5

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15 January 2018

Dominic Thyagarajan

6

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15 January 2018

publication date

1 June 2004

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15 January 2018

Journal of Clinical Neuroscience

published in

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15 January 2018

volume

11

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15 January 2018

issue

5

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15 January 2018

page(s)

537-539

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15 January 2018

The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0967-5868%2803%2900226-1

7 January 2021

The DYT1 phenotype and guidelines for diagnostic testing

1 reference

https://api.crossref.org/works/10.1016%2FS0967-5868%2803%2900226-1

7 January 2021

Spread of symptoms in idiopathic torsion dystonia

1 reference

https://api.crossref.org/works/10.1016%2FS0967-5868%2803%2900226-1

7 January 2021

The genetics of primary dystonias and related disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0967-5868%2803%2900226-1

7 January 2021

The role of DYT1 in primary torsion dystonia in Europe.

1 reference

https://api.crossref.org/works/10.1016%2FS0967-5868%2803%2900226-1

7 January 2021

Striatal dopamine in early-onset primary torsion dystonia with the DYT1 mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS0967-5868%2803%2900226-1

7 January 2021

Mutant torsinA, responsible for early-onset torsion dystonia, forms membrane inclusions in cultured neural cells

1 reference

https://api.crossref.org/works/10.1016%2FS0967-5868%2803%2900226-1

7 January 2021

Novel mutation in the TOR1A (DYT1) gene in atypical early onset dystonia and polymorphisms in dystonia and early onset parkinsonism.

1 reference

https://api.crossref.org/works/10.1016%2FS0967-5868%2803%2900226-1

7 January 2021

Clinical findings of a myoclonus-dystonia family with two distinct mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0967-5868%2803%2900226-1

7 January 2021

The DYT1 mutation and nonfamilial primary torsion dystonia

1 reference

https://api.crossref.org/works/10.1016%2FS0967-5868%2803%2900226-1

7 January 2021

Phenotypic expression of the DYT1 mutation: a family with writer's cramp of juvenile onset.

1 reference

https://api.crossref.org/works/10.1016%2FS0967-5868%2803%2900226-1

7 January 2021

Phenotypic variability of the DYT1 mutation in German dystonia patients

1 reference

https://api.crossref.org/works/10.1016%2FS0967-5868%2803%2900226-1

7 January 2021

The DYT1 GAG deletion is infrequent in sporadic and familial writer' s cramp

1 reference

https://api.crossref.org/works/10.1016%2FS0967-5868%2803%2900226-1

7 January 2021

10.1016/S0967-5868(03)00226-1

Identifiers

DOI

1 reference

15 January 2018

1 reference

15 January 2018