(Q44585784)

4 December 2017

A novel mutation in the C2 domain of protein kinase C gamma associated with spinocerebellar ataxia type 14. (English)

1 reference

4 December 2017

spinocerebellar ataxia

1 reference

Takehiro Ueda

1

1 reference

4 December 2017

Tsuneyoshi Seki

2

1 reference

4 December 2017

Kimitaka Katanazaka

3

1 reference

4 December 2017

Kenji Sekiguchi

4

1 reference

4 December 2017

Kazuhiro Kobayashi

5

1 reference

4 December 2017

Fumio Kanda

6

1 reference

4 December 2017

Tatsushi Toda

7

1 reference

4 December 2017

21 April 2013

1 reference

4 December 2017

1 reference

4 December 2017

260

1 reference

4 December 2017

6

1 reference

4 December 2017

1664-1666

1 reference

https://scigraph.springernature.com/pub.10.1007/s00415-013-6916-0

4 December 2017

0 references

cites work

Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond

1 reference

https://api.crossref.org/works/10.1007%2FS00415-013-6916-0

New mutations in protein kinase Cgamma associated with spinocerebellar ataxia type 14.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-013-6916-0

SCA14 in Norway, two families with autosomal dominant cerebellar ataxia and a novel mutation in the PRKCG gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-013-6916-0

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-013-6916-0

Enzymological analysis of mutant protein kinase Cgamma causing spinocerebellar ataxia type 14 and dysfunction in Ca2+ homeostasis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-013-6916-0

Mutation of the highly conserved cysteine residue 131 of the SCA14 associated PRKCG gene in a family with slow progressive cerebellar ataxia

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23604456

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S00415-013-6916-0

1 reference

4 December 2017

1 reference