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English
Exclusive cardiac dysfunction in familial primary carnitine deficiency cases: a genotype-phenotype correlation
scientific article published on 01 July 2007
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17594400
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17594400%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
title
Exclusive cardiac dysfunction in familial primary carnitine deficiency cases: a genotype-phenotype correlation
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17594400
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17594400%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
main subject
genotype-phenotype correlation
1 reference
based on heuristic
inferred from title
phenotype
1 reference
based on heuristic
inferred from title
author
Georges Nemer
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17594400
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17594400%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
author name string
A A Yamak
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17594400
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17594400%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
F Bitar
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17594400
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17594400%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
P Karam
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17594400
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17594400%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
publication date
1 July 2007
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17594400
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17594400%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
published in
Clinical Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17594400
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17594400%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
volume
72
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17594400
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17594400%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
issue
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17594400
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17594400%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
page(s)
59-62
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17594400
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17594400%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
Identifiers
DOI
10.1111/J.1399-0004.2007.00814.X
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17594400
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17594400%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
PubMed publication ID
17594400
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17594400
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17594400%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
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