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A novel nonsense mutation in the human dystrophin gene
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
8401539
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8401539%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
title
A novel nonsense mutation in the human dystrophin gene
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
8401539
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8401539%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
author
Marina Mora
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
8401539
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8401539%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
author name string
F A Saad
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
8401539
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8401539%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
G Vita
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
8401539
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8401539%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
L Morandi
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
8401539
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8401539%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
L Vitiello
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
8401539
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8401539%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
S Oliviero
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed ID
8401539
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8401539%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
G A Danieli
series ordinal
7
1 reference
stated in
Europe PubMed Central
PubMed ID
8401539
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8401539%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
publication date
1 January 1993
1 reference
stated in
Europe PubMed Central
PubMed ID
8401539
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8401539%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
published in
Human Mutation
1 reference
stated in
Europe PubMed Central
PubMed ID
8401539
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8401539%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
volume
2
1 reference
stated in
Europe PubMed Central
PubMed ID
8401539
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8401539%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
page(s)
314-316
1 reference
stated in
Europe PubMed Central
PubMed ID
8401539
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8401539%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
issue
4
1 reference
stated in
Europe PubMed Central
PubMed ID
8401539
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8401539%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
cites work
Point mutation in the human dystrophin gene: identification through western blot analysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380020413
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Premature chain termination mutation causing Duchenne muscular dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380020413
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Point mutations and polymorphisms in the human dystrophin gene identified in genomic DNA sequences amplified by multiplex PCR
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380020413
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Detection of a nonsense mutation in the dystrophin gene by multiple SSCP
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380020413
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Point mutations in the dystrophin gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380020413
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A 3' consensus splice mutation in the human dystrophin gene detected by a screening for intra-exonic deletions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380020413
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1002/HUMU.1380020413
1 reference
stated in
Europe PubMed Central
PubMed ID
8401539
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8401539%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
PubMed ID
8401539
1 reference
stated in
Europe PubMed Central
PubMed ID
8401539
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8401539%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
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