(Q34146067)

31 July 2017

title

Benign hereditary chorea of early onset maps to chromosome 14q. (English)

1 reference

31 July 2017

0 references

Benign hereditary chorea

1 reference

de Vries BB

1

1 reference

31 July 2017

Arts WF

2

1 reference

31 July 2017

Breedveld GJ

3

1 reference

31 July 2017

Hoogeboom JJ

4

1 reference

31 July 2017

Niermeijer MF

5

1 reference

31 July 2017

Heutink P

6

1 reference

31 July 2017

language of work or name

English

0 references

publication date

1 January 2000

1 reference

American Journal of Human Genetics

31 July 2017

language of work

1 reference

31 July 2017

volume

66

1 reference

31 July 2017

issue

1

1 reference

31 July 2017

page(s)

136-142

1 reference

The spinal muscular atrophy disease gene product, SMN, and its associated protein SIP1 are in a complex with spliceosomal snRNP proteins

31 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288318

Errors in Huntington disease diagnostic test caused by trinucleotide deletion in the IT15 gene.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288318

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288318

A worldwide study of the Huntington's disease mutation. The sensitivity and specificity of measuring CAG repeats

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288318

Identification of an expanded CAG repeat in the Huntington's disease gene (IT15) in a family reported to have benign hereditary chorea

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288318

Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288318

Benign familial chorea: an association with intellectual impairment

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288318

Benign familial chorea with onset in childhood

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288318

Hereditary nonprogressive chorea of early onset

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288318

Familial benign chorea with intention tremor: a clinical entity

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288318

A simple salting out procedure for extracting DNA from human nucleated cells

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288318

Hereditary progressive chorea without dementia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288318

Absence of close linkage between benign hereditary chorea and the locus D4S10 (probe G8)

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288318

Molecular Cloning and Expression of Biologically Active Human Glia Maturation Factor-?

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288318

Polyclonal antibody localizes glia maturation factor beta-like immunoreactivity in neurons and glia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288318

Benign hereditary chorea Clinical and genetic aspects

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288318

A Dutch family with benign hereditary chorea of early onset: differentiation from Huntington's disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288318

Expression of glia maturation factor beta mRNA and protein in rat organs and cells

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288318

Exclusion mapping of the benign hereditary chorea gene from the Huntington's disease locus: report of a family

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288318

28 October 2018

Benign hereditary chorea

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10631144

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Familial nonprogressive involuntary movements of childhood

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10631144

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/302725

1 reference

31 July 2017

1 reference

31 July 2017

1 reference