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English
Genetic heterogeneity in Leigh syndrome
scientific article published in July 1996
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8687192
retrieved
27 March 2018
reference URL
http://europepmc.org/abstract/MED/8687192
editorial
0 references
title
Genetic heterogeneity in Leigh syndrome
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8687192
retrieved
27 March 2018
reference URL
http://europepmc.org/abstract/MED/8687192
main subject
heterogeneity
1 reference
based on heuristic
inferred from title
author name string
DiMauro S
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8687192
retrieved
27 March 2018
reference URL
http://europepmc.org/abstract/MED/8687192
De Vivo DC
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8687192
retrieved
27 March 2018
reference URL
http://europepmc.org/abstract/MED/8687192
publication date
1 July 1996
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8687192
retrieved
27 March 2018
reference URL
http://europepmc.org/abstract/MED/8687192
published in
Annals of Neurology
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8687192
retrieved
27 March 2018
reference URL
http://europepmc.org/abstract/MED/8687192
volume
40
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8687192
retrieved
27 March 2018
reference URL
http://europepmc.org/abstract/MED/8687192
issue
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8687192
retrieved
27 March 2018
reference URL
http://europepmc.org/abstract/MED/8687192
page(s)
5-7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8687192
retrieved
27 March 2018
reference URL
http://europepmc.org/abstract/MED/8687192
cites work
Lacticacidemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FANA.410400104
retrieved
21 January 2018
Cytochrome c oxidase deficiency in Leigh's syndrome: genetic evidence for a nuclear DNA-encoded mutation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FANA.410400104
retrieved
21 January 2018
Clinical features associated with the A-->G transition at nucleotide 8344 of mtDNA ("MERRF mutation").
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FANA.410400104
retrieved
21 January 2018
Identifiers
DOI
10.1002/ANA.410400104
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8687192
retrieved
27 March 2018
reference URL
http://europepmc.org/abstract/MED/8687192
PubMed publication ID
8687192
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8687192
retrieved
27 March 2018
reference URL
http://europepmc.org/abstract/MED/8687192
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