(Q77929988)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10384394%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

title

Mutations in PEX1 in peroxisome biogenesis disorders: G843D and a mild clinical phenotype (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10384394%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

author name string

J Gärtner

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10384394%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

N Preuss

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10384394%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

U Brosius

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10384394%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

M Biermanns

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10384394%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

publication date

1 May 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10384394%20AND%20SRC:MED&resulttype=core&format=json

Journal of Inherited Metabolic Disease

9 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10384394%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

volume

22

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10384394%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10384394%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

page(s)

311-313

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10384394%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1023/a:1005599903632

9 December 2019

exact match

0 references

cites work

The sorting sequence of the peroxisomal integral membrane protein PMP47 is contained within a short hydrophilic loop

1 reference

12 December 2020

Mutations in the 70K peroxisomal membrane protein gene in Zellweger syndrome

1 reference

12 December 2020

A novel, cleavable peroxisomal targeting signal at the amino-terminus of the rat 3-ketoacyl-CoA thiolase

1 reference

12 December 2020

Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders

1 reference

12 December 2020

A conserved tripeptide sorts proteins to peroxisomes

1 reference

12 December 2020

Human PEX1 is mutated in complementation group 1 of the peroxisome biogenesis disorders

1 reference

12 December 2020