(Q45743755)

English

Novel ADAR1 mutations including a single amino acid deletion in the deaminase domain underlie dyschromatosis symmetrica hereditaria in Japanese families

scientific article published on 28 April 2013

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

15 December 2017

http://europepmc.org/abstract/MED/23621649

Novel ADAR1 mutations including a single amino acid deletion in the deaminase domain underlie dyschromatosis symmetrica hereditaria in Japanese families (English)

1 reference

Europe PubMed Central

PubMed publication ID

15 December 2017

http://europepmc.org/abstract/MED/23621649

dyschromatosis symmetrica hereditaria

0 references

author name string

Michihiro Kono

1

1 reference

Europe PubMed Central

PubMed publication ID

15 December 2017

http://europepmc.org/abstract/MED/23621649

Mutsumi Suganuma

2

1 reference

Europe PubMed Central

PubMed publication ID

15 December 2017

http://europepmc.org/abstract/MED/23621649

Masashi Akiyama

3

1 reference

Europe PubMed Central

PubMed publication ID

15 December 2017

http://europepmc.org/abstract/MED/23621649

Yasutomo Ito

4

1 reference

Europe PubMed Central

PubMed publication ID

15 December 2017

http://europepmc.org/abstract/MED/23621649

Hideyuki Ujiie

5

1 reference

Europe PubMed Central

PubMed publication ID

15 December 2017

http://europepmc.org/abstract/MED/23621649

Kenichi Morimoto

6

1 reference

Europe PubMed Central

PubMed publication ID

15 December 2017

http://europepmc.org/abstract/MED/23621649

publication date

28 April 2013

1 reference

Europe PubMed Central

PubMed publication ID

15 December 2017

http://europepmc.org/abstract/MED/23621649

International Journal of Dermatology

1 reference

Europe PubMed Central

PubMed publication ID

15 December 2017

http://europepmc.org/abstract/MED/23621649

53

1 reference

Europe PubMed Central

PubMed publication ID

15 December 2017

http://europepmc.org/abstract/MED/23621649

3

1 reference

Europe PubMed Central

PubMed publication ID

15 December 2017

http://europepmc.org/abstract/MED/23621649

e194-6

1 reference

Europe PubMed Central

PubMed publication ID

15 December 2017

http://europepmc.org/abstract/MED/23621649

Exclusion of linkage between dyschromatosis symmetrica hereditaria and chromosome 9.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-4632.2012.05765.X

21 January 2018

Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-4632.2012.05765.X

21 January 2018

Cloning of cDNAs encoding mammalian double-stranded RNA-specific adenosine deaminase

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-4632.2012.05765.X

21 January 2018

Mutation analysis of the ADAR1 gene in dyschromatosis symmetrica hereditaria and genetic differentiation from both dyschromatosis universalis hereditaria and acropigmentatio reticularis

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-4632.2012.05765.X

21 January 2018

Two novel mutations and evidence for haploinsufficiency of the ADAR gene in dyschromatosis symmetrica hereditaria

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-4632.2012.05765.X

21 January 2018

A rule for termination-codon position within intron-containing genes: when nonsense affects RNA abundance

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-4632.2012.05765.X

21 January 2018

Identifiers

10.1111/J.1365-4632.2012.05765.X

1 reference

Europe PubMed Central

PubMed publication ID

15 December 2017

http://europepmc.org/abstract/MED/23621649

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

15 December 2017

http://europepmc.org/abstract/MED/23621649

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