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English
Haplotypes and mutations in Wilson disease.
scientific article published on June 1995
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1801091
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762553%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 October 2019
title
Haplotypes and mutations in Wilson disease
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1801091
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762553%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 October 2019
author name string
Thomas GR
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1801091
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762553%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 October 2019
Roberts EA
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1801091
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762553%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 October 2019
Walshe JM
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
1801091
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762553%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 October 2019
Cox DW
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMC publication ID
1801091
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762553%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 October 2019
language of work or name
English
0 references
publication date
1 June 1995
1 reference
stated in
Europe PubMed Central
PMC publication ID
1801091
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762553%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 October 2019
published in
American Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
1801091
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762553%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 October 2019
volume
56
1 reference
stated in
Europe PubMed Central
PMC publication ID
1801091
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762553%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 October 2019
issue
6
1 reference
stated in
Europe PubMed Central
PMC publication ID
1801091
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762553%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 October 2019
page(s)
1315-1319
1 reference
stated in
Europe PubMed Central
PMC publication ID
1801091
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762553%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 October 2019
cites work
The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene
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=1801091
retrieved
27 July 2018
Mapping, cloning and genetic characterization of the region containing the Wilson disease gene.
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=1801091
retrieved
27 July 2018
The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene
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=1801091
retrieved
27 July 2018
Haplotype studies in Wilson disease
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=1801091
retrieved
27 July 2018
A simple salting out procedure for extracting DNA from human nucleated cells
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=1801091
retrieved
27 July 2018
Friedreich ataxia in Louisiana Acadians: demonstration of a founder effect by analysis of microsatellite-generated extended haplotypes
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=1801091
retrieved
27 July 2018
Dinucleotide repeat polymorphisms at the SCN4A locus suggest allelic heterogeneity of hyperkalemic periodic paralysis and paramyotonia congenita
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=1801091
retrieved
27 July 2018
Linkage disequilibrium between the fragile X mutation and two closely linked CA repeats suggests that fragile X chromosomes are derived from a small number of founder chromosomes
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=1801091
retrieved
25 September 2018
Wilson disease in Iceland: a clinical and genetic study.
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=1801091
retrieved
25 September 2018
The Wilson disease gene: spectrum of mutations and their consequences
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=1801091
retrieved
25 September 2018
Wilson's disease in Israel: a genetic and epidemiological study
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=1801091
retrieved
25 September 2018
DNA markers for the diagnosis of Wilson disease
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7762553
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Allelic association and linkage studies in Wilson disease
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7762553
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Wilson disease
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7762553
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
PMC publication ID
1801091
1 reference
stated in
Europe PubMed Central
PMC publication ID
1801091
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762553%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 October 2019
PubMed publication ID
7762553
1 reference
stated in
Europe PubMed Central
PMC publication ID
1801091
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762553%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 October 2019
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