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English
Predicted homozygous mis-sense mutation in Gilbert's syndrome
scientific article published on 01 December 1995
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7491021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7491021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
title
Predicted homozygous mis-sense mutation in Gilbert's syndrome
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7491021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7491021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
main subject
homozygosity
1 reference
based on heuristic
inferred from title
author name string
Y Soeda
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7491021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7491021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
K Yamamoto
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7491021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7491021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
Y Adachi
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7491021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7491021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
T Hori
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7491021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7491021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
S Aono
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7491021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7491021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
O Koiwai
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7491021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7491021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
H Sato
series ordinal
7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7491021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7491021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
language of work or name
English
0 references
publication date
1 December 1995
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7491021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7491021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
published in
The Lancet
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7491021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7491021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
volume
346
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7491021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7491021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
issue
8988
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7491021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7491021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
page(s)
1494
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7491021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7491021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
cites work
Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2895%2992514-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Gilbert's syndrome is caused by a heterozygous missense mutation in the gene for bilirubin UDP-glucuronosyltransferase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2895%2992514-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of defect in the genes for bilirubin UDP-glucuronosyl-transferase in a patient with Crigler-Najjar syndrome type II
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2895%2992514-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0140-6736(95)92514-7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7491021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7491021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
PubMed publication ID
7491021
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7491021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7491021%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
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