(Q48612182)

13 February 2018

title

Novel PRKCG/SCA14 mutation in a Dutch spinocerebellar ataxia family: expanding the phenotype. (English)

1 reference

13 February 2018

main subject

spinocerebellar ataxia

1 reference

1 reference

Monique H M Vlak

1

1 reference

13 February 2018

Richard J Sinke

2

1 reference

13 February 2018

Gwenda M Rabelink

3

1 reference

13 February 2018

Berry P H Kremer

4

1 reference

13 February 2018

Bart P C van de Warrenburg

5

1 reference

13 February 2018

language of work or name

English

0 references

publication date

1 July 2006

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13 February 2018

published in

Movement Disorders

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13 February 2018

volume

21

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13 February 2018

issue

7

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13 February 2018

page(s)

1025-1028

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13 February 2018

Missense mutations in the regulatory domain of PKC gamma: a new mechanism for dominant nonepisodic cerebellar ataxia

cites work

1 reference

https://api.crossref.org/works/10.1002%2FMDS.20851

Crossref

reference URL

retrieved

21 January 2018

Spinocerebellar ataxia type 14 caused by a mutation in protein kinase C gamma

1 reference

https://api.crossref.org/works/10.1002%2FMDS.20851

Crossref

reference URL

retrieved

21 January 2018

Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14.

1 reference

https://api.crossref.org/works/10.1002%2FMDS.20851

Crossref

reference URL

retrieved

21 January 2018

Identifiers

DOI

10.1002/MDS.20851

1 reference

13 February 2018

PubMed ID

16547918

1 reference

13 February 2018