(Q81449602)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17940722%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

title

Screening of the SPTBN2 (SCA5) gene in German SCA patients (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17940722%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

author name string

C Zühlke

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17940722%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

V Bernard

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17940722%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

A Dalski

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17940722%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

P Lorenz

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17940722%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

B Mitulla

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17940722%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

G Gillessen-Kaesbach

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17940722%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

K Bürk

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17940722%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

publication date

25 October 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17940722%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17940722%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

volume

254

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17940722%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

issue

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17940722%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

page(s)

1649-1652

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17940722%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00415-007-0600-1

8 January 2020

exact match

0 references

cites work

Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypes

1 reference

12 December 2020

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

1 reference

12 December 2020

Spinocerebellar ataxia type 5: clinical and molecular genetic features of a German kindred.

1 reference

12 December 2020

Clinical and MRI findings in spinocerebellar ataxia type 5

1 reference

12 December 2020

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

1 reference

12 December 2020

Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia family

1 reference

12 December 2020

The clinical and genetic spectrum of spinocerebellar ataxia 14

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

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

1 reference

12 December 2020

Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11.

1 reference

12 December 2020

The wide spectrum of spinocerebellar ataxias (SCAs)

1 reference

12 December 2020

Spectrin mutations cause spinocerebellar ataxia type 5.

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