(Q58850960)

3

Jean Mathieu

0 references

Andrea M. Richter

2

Andrea Richter

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Serge B. Melançon

7

Serge B Melançon

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Kenneth Morgan

6

Kenneth Morgan

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Thomas J. Hudson

5

Thomas J Hudson

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author name string

Denis Brunet

The Troyer syndrome. A recessive form of spastic paraplegia with distal muscle wasting

4

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language of work or name

English

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publication date

October 1998

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published in

Neuromuscular Disorders

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volume

8

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issue

7

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page(s)

474-479

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cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900055-8

7 January 2021

New type of spinocerebellar degeneration syndrome in a northern Swedish population

1 reference

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7 January 2021

Autosomally inherited recessive spastic ataxia, macular corneal dystrophy, congenital cataracts, myopia and vertically oval temporally tilted discs. Report of a Bedouin family--a new syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900055-8

7 January 2021

Genetic epidemiology of autosomal recessive spastic ataxia of Charlevoix-Saguenay in northeastern Quebec

1 reference

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7 January 2021

Electroencephalographic Findings in Friedreich's Ataxia and Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS)

1 reference

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7 January 2021

Electromyography and Nerve Conduction Studies in Friedreich's Ataxia and Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS)

1 reference

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7 January 2021

The Neuropathy of Charlevoix-Saguenay Ataxia: An Electrophysiological and Pathological Study

1 reference

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7 January 2021

Oculomotor and Vestibular Findings in Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2898%2900055-8

7 January 2021

Computed Tomography of Posterior Fossa in Hereditary Ataxias

1 reference

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7 January 2021

The 1993-94 Généthon human genetic linkage map

1 reference

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7 January 2021

Strategies for multilocus linkage analysis in humans

1 reference

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7 January 2021

Sets of short tandem repeat polymorphisms for efficient linkage screening of the human genome

1 reference

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7 January 2021

Electrophysiological studies in familial spastic paraplegia

1 reference

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7 January 2021