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Mitochondrial disorders: clinical and genetic features
scientific article
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
10073267
retrieved
27 July 2017
review article
1 reference
stated in
Europe PubMed Central
title
Mitochondrial disorders: clinical and genetic features
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
10073267
retrieved
27 July 2017
main subject
mitochondrion
1 reference
based on heuristic
inferred from title
author name string
Simon DK
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
10073267
retrieved
27 July 2017
Johns DR
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
10073267
retrieved
27 July 2017
publication date
1 January 1999
1 reference
stated in
Europe PubMed Central
PubMed ID
10073267
retrieved
27 July 2017
published in
Annual Review of Medicine
1 reference
stated in
Europe PubMed Central
PubMed ID
10073267
retrieved
27 July 2017
volume
50
1 reference
stated in
Europe PubMed Central
PubMed ID
10073267
retrieved
27 July 2017
page(s)
111-127
1 reference
stated in
Europe PubMed Central
PubMed ID
10073267
retrieved
27 July 2017
issue
1
1 reference
retrieved
28 June 2019
cites work
Mutations in mitochondrial cytochrome c oxidase genes segregate with late-onset Alzheimer disease
1 reference
stated in
COCI
retrieved
12 January 2024
reference URL
https://opencitations.net/index/api/v1/citations/10.1073/PNAS.94.9.4526
Identifiers
DOI
10.1146/ANNUREV.MED.50.1.111
1 reference
stated in
Europe PubMed Central
PubMed ID
10073267
retrieved
27 July 2017
PubMed ID
10073267
1 reference
stated in
Europe PubMed Central
PubMed ID
10073267
retrieved
27 July 2017
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