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Spinocerebellar ataxia type 23: a genetic update
scientific article published on 17 December 2008
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
2694919
retrieved
19 August 2017
review article
1 reference
stated in
Europe PubMed Central
title
Spinocerebellar ataxia type 23: a genetic update
(English)
1 reference
stated in
Europe PubMed Central
PMCID
2694919
retrieved
19 August 2017
main subject
spinocerebellar ataxia type 23
1 reference
based on heuristic
inferred from title
author name string
Dineke S Verbeek
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
2694919
retrieved
19 August 2017
publication date
17 December 2008
1 reference
stated in
Europe PubMed Central
PMCID
2694919
retrieved
19 August 2017
published in
The Cerebellum
1 reference
stated in
Europe PubMed Central
PMCID
2694919
retrieved
19 August 2017
volume
8
1 reference
stated in
Europe PubMed Central
PMCID
2694919
retrieved
19 August 2017
issue
2
1 reference
stated in
Europe PubMed Central
PMCID
2694919
retrieved
19 August 2017
page(s)
104-107
1 reference
stated in
Europe PubMed Central
PMCID
2694919
retrieved
19 August 2017
exact match
https://scigraph.springernature.com/pub.10.1007/s12311-008-0085-1
0 references
cites work
Spinocerebellar ataxia type 28: a novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694919
retrieved
6 September 2017
Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694919
retrieved
6 September 2017
Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694919
retrieved
6 September 2017
A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694919
retrieved
6 September 2017
Reconstruction of a functional human gene network, with an application for prioritizing positional candidate genes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694919
retrieved
6 September 2017
Molecular pathogenesis of spinocerebellar ataxias.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694919
retrieved
6 September 2017
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
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694919
retrieved
6 September 2017
Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694919
retrieved
6 September 2017
Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694919
retrieved
6 September 2017
Classification of the hereditary ataxias and paraplegias
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694919
retrieved
6 September 2017
Autosomal dominant congenital non-progressive ataxia overlaps with the SCA15 locus
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694919
retrieved
3 September 2018
Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694919
retrieved
3 September 2018
The hereditary adult-onset ataxias in South Africa
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694919
retrieved
3 September 2018
Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locus.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694919
retrieved
3 September 2018
Spinocerebellar ataxias in the Netherlands: prevalence and age at onset variance analysis.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2694919
retrieved
3 September 2018
Molecular analysis of autosomal dominant hereditary ataxias in the Indian population: high frequency of SCA2 and evidence for a common founder mutation
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/19089525
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1007/S12311-008-0085-1
1 reference
stated in
Europe PubMed Central
PMCID
2694919
retrieved
19 August 2017
PMCID
2694919
1 reference
stated in
Europe PubMed Central
PMCID
2694919
retrieved
19 August 2017
PubMed ID
19089525
1 reference
stated in
Europe PubMed Central
PMCID
2694919
retrieved
19 August 2017
ResearchGate publication ID
23670411
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