(Q46156839)

English

H syndrome with a novel homozygous R134C mutation in SLC29A3 gene

scientific article published in July 2013

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/23789599

H syndrome with a novel homozygous R134C mutation in SLC29A3 gene (English)

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/23789599

1 reference

based on heuristic

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1 reference

based on heuristic

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Robert K Semple

3

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/23789599

Devinder Mohan Thappa

4

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/23789599

Laxmisha Chandrashekar

object named as

Laxmisha Chandrashekar

2

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Saritha Mohanan

1

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/23789599

Nachiappa Ganesh Rajesh

5

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/23789599

Vir S Negi

6

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/23789599

Reena Gulati

7

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/23789599

publication date

1 July 2013

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/23789599

International Journal of Dermatology

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/23789599

52

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/23789599

7

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/23789599

820-823

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/23789599

H syndrome: novel and recurrent mutations in SLC29A3.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-4632.2012.05838.X

21 January 2018

SLC29A3 gene is mutated in pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome and interacts with the insulin signaling pathway.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-4632.2012.05838.X

21 January 2018

The H syndrome is caused by mutations in the nucleoside transporter hENT3.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-4632.2012.05838.X

21 January 2018

The H syndrome: two novel mutations affecting the same amino acid residue of hENT3.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-4632.2012.05838.X

21 January 2018

A case of H syndrome showing immunophenotye similarities to Rosai-Dorfman disease.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-4632.2012.05838.X

21 January 2018

Identifiers

10.1111/J.1365-4632.2012.05838.X

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/23789599

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/23789599

ResearchGate publication ID

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