(Q47889879)

English

Different phenotypes of Friedreich's ataxia within one 'pseudo-dominant' genealogy: relationships between trinucleotide (GAA) repeat lengths and clinical features

scientific article published in September 2000

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/11054139

Different phenotypes of Friedreich's ataxia within one 'pseudo-dominant' genealogy: relationships between trinucleotide (GAA) repeat lengths and clinical features (English)

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/11054139

Friedreich ataxia

1 reference

based on heuristic

inferred from title

author name string

S N Illarioshkin

1

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/11054139

G K Bagieva

2

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/11054139

S A Klyushnikov

3

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/11054139

I V Ovchinnikov

4

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/11054139

E D Markova

5

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/11054139

I A Ivanova-Smolenskaya

6

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/11054139

publication date

1 September 2000

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/11054139

European Journal of Neurology

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/11054139

7

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/11054139

5

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/11054139

535-540

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/11054139

Identification and sizing of the GAA trinucleotide repeat expansion of Friedreich's ataxia in 56 patients. Clinical and genetic correlates

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2000.T01-1-00113.X

21 January 2018

Mapping of mutation causing Friedreich's ataxia to human chromosome 9

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2000.T01-1-00113.X

21 January 2018

Clinical Description and Roentgenologic Evaluation of Patients with Friedreich's Ataxia

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2000.T01-1-00113.X

21 January 2018

Locus heterogeneity in Friedreich ataxia

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2000.T01-1-00113.X

21 January 2018

Broadened Friedreich's ataxia phenotype after gene cloning. Minimal GAA expansion causes late-onset spastic ataxia

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2000.T01-1-00113.X

21 January 2018

Identifiers

10.1046/J.1468-1331.2000.T01-1-00113.X

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/11054139

release_4iat4aso2ngh5mkee3np4scwte

1 reference

https://api.fatcat.wiki/v0/release/4iat4aso2ngh5mkee3np4scwte

24 November 2022

based on heuristic

mapped directly with Wikidata item

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/11054139

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=Q47889879&oldid=2174846314"