R58fs mutation in the HGD gene in a family with alkaptonuria in the UAE. (Q46020000)

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scientific article published on 20 October 2008

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Language	Label	Description	Also known as
English	R58fs mutation in the HGD gene in a family with alkaptonuria in the UAE.	scientific article published on 20 October 2008

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18945288

retrieved

18 December 2017

reference URL

http://europepmc.org/abstract/MED/18945288

title

R58fs mutation in the HGD gene in a family with alkaptonuria in the UAE. (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18945288

retrieved

18 December 2017

reference URL

http://europepmc.org/abstract/MED/18945288

main subject

alkaptonuria

1 reference

based on heuristic

inferred from title

author

Bassam R. Ali

object named as

Bassam R Ali

series ordinal

5

0 references

author name string

Yousef M Abdulrazzaq

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18945288

retrieved

18 December 2017

reference URL

http://europepmc.org/abstract/MED/18945288

Ahmed Ibrahim

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18945288

retrieved

18 December 2017

reference URL

http://europepmc.org/abstract/MED/18945288

Abdullah I Al-Khayat

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18945288

retrieved

18 December 2017

reference URL

http://europepmc.org/abstract/MED/18945288

Nicolaas Nagelkerke

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18945288

retrieved

18 December 2017

reference URL

http://europepmc.org/abstract/MED/18945288

language of work or name

English

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publication date

20 October 2008

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18945288

retrieved

18 December 2017

reference URL

http://europepmc.org/abstract/MED/18945288

published in

Annals of Human Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18945288

retrieved

18 December 2017

reference URL

http://europepmc.org/abstract/MED/18945288

volume

73

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18945288

retrieved

18 December 2017

reference URL

http://europepmc.org/abstract/MED/18945288

issue

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18945288

retrieved

18 December 2017

reference URL

http://europepmc.org/abstract/MED/18945288

page(s)

125-130

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18945288

retrieved

18 December 2017

reference URL

http://europepmc.org/abstract/MED/18945288

cites work

High frequency of alkaptonuria in Slovakia: evidence for the appearance of multiple mutations in HGO involving different mutational hot spots

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2008.00485.X

retrieved

21 January 2018

Molecular analyses of the HGO gene mutations in Turkish alkaptonuria patients suggest that the R58fs mutation originated from central Asia and was spread throughout Europe and Anatolia by human migrations

1 reference

stated in

COCI

retrieved

9 November 2024

reference URL

https://opencitations.net/index/api/v1/citations/10.1023/A:1024063126954

Identifiers

DOI

10.1111/J.1469-1809.2008.00485.X

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18945288

retrieved

18 December 2017

reference URL

http://europepmc.org/abstract/MED/18945288

PubMed publication ID

18945288

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18945288

retrieved

18 December 2017

reference URL

http://europepmc.org/abstract/MED/18945288

ResearchGate publication ID

23409268

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