(Q41937880)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19471976%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

title

SCA27 caused by a chromosome translocation: further delineation of the phenotype (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19471976%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19471976%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

author name string

D Misceo

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19471976%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

M Fannemel

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19471976%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

T Barøy

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19471976%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

R Roberto

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19471976%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

B Tvedt

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19471976%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

T Jaeger

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19471976%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

V Bryn

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19471976%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

P Strømme

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19471976%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

publication date

27 May 2009

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19471976%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19471976%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

volume

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19471976%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19471976%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

page(s)

371-374

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19471976%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s10048-009-0197-x

29 January 2020

exact match

0 references

cites work

Spinocerebellar ataxia associated with a mutation in the fibroblast growth factor 14 gene (SCA27): A new phenotype

1 reference

12 December 2020

Subcellular and developmental expression of alternatively spliced forms of fibroblast growth factor 14.

1 reference

12 December 2020

Fibroblast growth factor (FGF) homologous factors: new members of the FGF family implicated in nervous system development

1 reference

12 December 2020

The FGF14(F145S) mutation disrupts the interaction of FGF14 with voltage-gated Na+ channels and impairs neuronal excitability

1 reference

12 December 2020

Ataxia and paroxysmal dyskinesia in mice lacking axonally transported FGF14.

1 reference

12 December 2020

Mutation analysis in the fibroblast growth factor 14 gene: frameshift mutation and polymorphisms in patients with inherited ataxias

1 reference

12 December 2020

Impaired spatial learning and defective theta burst induced LTP in mice lacking fibroblast growth factor 14

1 reference

12 December 2020

A mutation in the fibroblast growth factor 14 gene is associated with autosomal dominant cerebellar ataxia [corrected]

1 reference

12 December 2020