(Q48354697)

English

Multiple system atrophy in a patient with the spinocerebellar ataxia 3 gene mutation.

scientific article published in January 2007

In more languages

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/17133518

Multiple system atrophy in a patient with the spinocerebellar ataxia 3 gene mutation. (English)

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/17133518

1 reference

based on heuristic

inferred from title

multiple system atrophy

1 reference

based on heuristic

inferred from title

spinocerebellar ataxia

1 reference

based on heuristic

inferred from title

Melissa J Nirenberg

1

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/17133518

2

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/17133518

4

object named as

Stanley Fahn

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

author name string

Jean-Paul Vonsattel

3

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/17133518

language of work or name

0 references

publication date

1 January 2007

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/17133518

Movement Disorders

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/17133518

22

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/17133518

2

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/17133518

251-254

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/17133518

Multiple-system atrophy is genetically distinct from identified inherited causes of spinocerebellar degeneration

1 reference

https://api.crossref.org/works/10.1002%2FMDS.21231

21 January 2018

Identifiers

10.1002/MDS.21231

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/17133518

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/17133518

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