(Q58477856)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17549529%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

title

Age at onset in sod1-mediated amyotrophic lateral sclerosis shows familiality (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17549529%20AND%20SRC:MED&resulttype=core&format=json

amyotrophic lateral sclerosis

31 December 2019

main subject

0 references

author

Isabella Fogh

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17549529%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Fruhling Rijsdijk

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17549529%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Jo Knight

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17549529%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Vincenzo Silani

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17549529%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Ammar Al-Chalabi

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17549529%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

6

Benjamin Neale

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17549529%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

9

Robert H Brown

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17549529%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

author name string

Diane McKenna-Yasek

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17549529%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Peter M Andersen

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17549529%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Pak C Sham

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17549529%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

John F Powell

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17549529%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

publication date

5 June 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17549529%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17549529%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

volume

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17549529%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17549529%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

page(s)

235-236

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17549529%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s10048-007-0092-2

31 December 2019

exact match

0 references

cites work

Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset

1 reference

12 December 2020

Linkage of type 2 diabetes mellitus and of age at onset to a genetic location on chromosome 10q in Mexican Americans

1 reference

12 December 2020

Age at onset in two common neurodegenerative diseases is genetically controlled

1 reference

12 December 2020

A shared chromosome-21 haplotype among amyotrophic lateral sclerosis families with the A4V SOD1 mutation

1 reference

12 December 2020

A frequent ala 4 to val superoxide dismutase-1 mutation is associated with a rapidly progressive familial amyotrophic lateral sclerosis

1 reference

12 December 2020

Autosomal recessive adult-onset amyotrophic lateral sclerosis associated with homozygosity for Asp90Ala CuZn-superoxide dismutase mutation. A clinical and genealogical study of 36 patients

1 reference

12 December 2020

10.1007/S10048-007-0092-2

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17549529%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

1 reference