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English
Novel cardiac beta-myosin heavy chain gene missense mutations (R869C and R870C) that cause familial hypertrophic cardiomyopathy
scientific article published on 01 June 2000
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10862102
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10862102%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
title
Novel cardiac beta-myosin heavy chain gene missense mutations (R869C and R870C) that cause familial hypertrophic cardiomyopathy
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10862102
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10862102%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
main subject
hypertrophic cardiomyopathy
1 reference
based on heuristic
inferred from title
familial hypertrophic cardiomyopathy
1 reference
based on heuristic
inferred from title
author name string
Anan R
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10862102
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10862102%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
Shono H
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10862102
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10862102%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
Tei C
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10862102
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10862102%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
publication date
1 June 2000
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10862102
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10862102%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
published in
Human Mutation
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10862102
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10862102%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
volume
15
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10862102
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10862102%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
issue
6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10862102
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10862102%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
page(s)
584
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10862102
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10862102%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
Identifiers
DOI
10.1002/1098-1004(200006)15:6<584::AID-HUMU25>3.0.CO;2-R
0 references
PubMed publication ID
10862102
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10862102
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10862102%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
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