(Q47235885)

English

A clinical and genetic study of 56 Saudi Wilson disease patients: identification of Saudi-specific mutations

scientific article published in February 2004

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/14748773

A clinical and genetic study of 56 Saudi Wilson disease patients: identification of Saudi-specific mutations (English)

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/14748773

1 reference

based on heuristic

inferred from title

author name string

M Al Jumah

1

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/14748773

R Majumdar

2

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/14748773

S Al Rajeh

3

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/14748773

A Awada

4

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/14748773

A Al Zaben

5

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/14748773

I Al Traif

6

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/14748773

A R Al Jumah

7

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/14748773

Z Rehana

8

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/14748773

publication date

1 February 2004

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/14748773

European Journal of Neurology

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/14748773

11

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/14748773

2

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/14748773

121-124

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/14748773

Mutation analysis and the correlation between genotype and phenotype of Arg778Leu mutation in chinese patients with Wilson disease

1 reference

https://api.crossref.org/works/10.1046%2FJ.1351-5101.2003.00729.X

21 January 2018

A study of Wilson disease mutations in Britain

1 reference

https://api.crossref.org/works/10.1046%2FJ.1351-5101.2003.00729.X

21 January 2018

Wilson disease mutations associated with uncommon haplotypes in Mediterranean patients

1 reference

https://api.crossref.org/works/10.1046%2FJ.1351-5101.2003.00729.X

21 January 2018

A novel deletion mutation within the carboxyl terminus of the copper-transporting ATPase gene causes Wilson disease

1 reference

https://api.crossref.org/works/10.1046%2FJ.1351-5101.2003.00729.X

21 January 2018

Identifiers

10.1046/J.1351-5101.2003.00729.X

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/14748773

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/14748773

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q47235885&oldid=2147248772"