(Q59697192)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18563470%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

title

Hereditary spastic paraplegia caused by the novel mutation 1047insC in the SPG7 gene (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18563470%20AND%20SRC:MED&resulttype=core&format=json

hereditary spastic paraplegia

9 January 2020

main subject

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18563470%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Laurence Bindoff

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18563470%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Filippo Maria Santorelli

series ordinal

3

object named as

Filippo M Santorelli

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18563470%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

author name string

Paola S Denora

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18563470%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

publication date

23 June 2008

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18563470%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18563470%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

volume

255

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18563470%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

issue

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18563470%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

page(s)

1142-1144

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18563470%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00415-008-0858-y

9 January 2020

exact match

0 references

cites work

The m-AAA protease defective in hereditary spastic paraplegia controls ribosome assembly in mitochondria

1 reference

12 December 2020

Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease

1 reference

12 December 2020

A clinical, genetic and biochemical study of SPG7 mutations in hereditary spastic paraplegia

1 reference

12 December 2020

Hereditary spastic paraparesis: a review of new developments.

1 reference

12 December 2020

Genew: the Human Gene Nomenclature Database, 2004 updates

1 reference

12 December 2020

A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3

1 reference

12 December 2020

Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegia

1 reference

12 December 2020

10.1007/S00415-008-0858-Y

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18563470%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

1 reference