Focal Palmoplantar Keratoderma Caused by an Autosomal Dominant Inherited Mutation in the Desmoglein 1 Gene (Q58859851)

From Wikidata

Jump to navigation Jump to search

article

edit

Language	Label	Description	Also known as
English	Focal Palmoplantar Keratoderma Caused by an Autosomal Dominant Inherited Mutation in the Desmoglein 1 Gene	article

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16484817

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16484817%20AND%20SRC:MED&resulttype=core&format=json

retrieved

17 January 2020

title

Focal palmoplantar keratoderma caused by an autosomal dominant inherited mutation in the desmoglein 1 gene (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16484817

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16484817%20AND%20SRC:MED&resulttype=core&format=json

retrieved

17 January 2020

author

Irwin McLean

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16484817

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16484817%20AND%20SRC:MED&resulttype=core&format=json

retrieved

17 January 2020

author name string

M Milingou

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16484817

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16484817%20AND%20SRC:MED&resulttype=core&format=json

retrieved

17 January 2020

P Wood

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16484817

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16484817%20AND%20SRC:MED&resulttype=core&format=json

retrieved

17 January 2020

I Masouyé

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16484817

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16484817%20AND%20SRC:MED&resulttype=core&format=json

retrieved

17 January 2020

L Borradori

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16484817

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16484817%20AND%20SRC:MED&resulttype=core&format=json

retrieved

17 January 2020

publication date

1 January 2006

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16484817

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16484817%20AND%20SRC:MED&resulttype=core&format=json

retrieved

17 January 2020

published in

Dermatology

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16484817

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16484817%20AND%20SRC:MED&resulttype=core&format=json

retrieved

17 January 2020

volume

212

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16484817

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16484817%20AND%20SRC:MED&resulttype=core&format=json

retrieved

17 January 2020

issue

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16484817

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16484817%20AND%20SRC:MED&resulttype=core&format=json

retrieved

17 January 2020

page(s)

117-122

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16484817

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16484817%20AND%20SRC:MED&resulttype=core&format=json

retrieved

17 January 2020

cites work

Human keratin diseases: the increasing spectrum of disease and subtlety of the phenotype-genotype correlation

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1159%2F000090651

retrieved

21 January 2018

Phenotypes, genotypes and their contribution to understanding keratin function

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1159%2F000090651

retrieved

21 January 2018

Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1159%2F000090651

retrieved

21 January 2018

Autoantibodies against a novel epithelial cadherin in pemphigus vulgaris, a disease of cell adhesion

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1159%2F000090651

retrieved

21 January 2018

Identifiers

DOI

10.1159/000090651

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16484817

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16484817%20AND%20SRC:MED&resulttype=core&format=json

retrieved

17 January 2020

PubMed publication ID

16484817

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16484817

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16484817%20AND%20SRC:MED&resulttype=core&format=json

retrieved

17 January 2020

 

Sitelinks

Wikipedia(0 entries)

edit

Wikibooks(0 entries)

edit

Wikinews(0 entries)

edit

Wikiquote(0 entries)

edit

Wikisource(0 entries)

edit

Wikiversity(0 entries)

edit

Wikivoyage(0 entries)

edit

Wiktionary(0 entries)

edit

Multilingual sites(0 entries)

edit

Retrieved from "https://www.wikidata.org/w/index.php?title=Q58859851&oldid=1495512987"