(Q34496428)

English

Mutations of the puratrophin-1 (PLEKHG4) gene on chromosome 16q22.1 are not a common genetic cause of cerebellar ataxia in a European population

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Mutations of the puratrophin-1 (PLEKHG4) gene on chromosome 16q22.1 are not a common genetic cause of cerebellar ataxia in a European population (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

cerebellar ataxia

1 reference

based on heuristic

inferred from title

author name string

Stefan Wieczorek

1

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Larissa Arning

2

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Ingrid Alheite

3

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Jörg T Epplen

4

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

publication date

21 February 2006

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Europe PubMed Central

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2 August 2017

Journal of Human Genetics

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Europe PubMed Central

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2 August 2017

51

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Europe PubMed Central

PubMed publication ID

2 August 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

363-367

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

https://scigraph.springernature.com/pub.10.1007/s10038-006-0372-y

0 references

Association of the HLA region with multiple sclerosis as confirmed by a genome screen using >10,000 SNPs on DNA chips

1 reference

https://pubmed.ncbi.nlm.nih.gov/16491300

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spinocerebellar ataxia type 14 caused by a mutation in protein kinase C gamma

1 reference

https://pubmed.ncbi.nlm.nih.gov/16491300

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16491300

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1

1 reference

https://pubmed.ncbi.nlm.nih.gov/16491300

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A gene on SCA4 locus causes dominantly inherited pure cerebellar ataxia

1 reference

https://pubmed.ncbi.nlm.nih.gov/16491300

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spinocerebellar ataxia type 4. Investigation of 34 candidate genes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16491300

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22-q11.2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16491300

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymerase chain reaction—single strand conformation polymorphism or how to detect reliably and efficiently each sequence variation in many samples and many genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/16491300

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The pathogenesis of spinocerebellar ataxia

1 reference

https://pubmed.ncbi.nlm.nih.gov/16491300

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor dom

1 reference

https://pubmed.ncbi.nlm.nih.gov/16491300

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia family

1 reference

https://pubmed.ncbi.nlm.nih.gov/16491300

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Refinement of the spinocerebellar ataxia type 4 locus in a large German family and exclusion of CAG repeat expansions in this region

1 reference

https://pubmed.ncbi.nlm.nih.gov/16491300

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10038-006-0372-Y

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

ResearchGate publication ID

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