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Hereditary and biochemical research in mitochondrial encefalomyopathies.
Lissens, Willy
(Co-Promotor)
De Meirleir, Linda
(Coördinator)
De Meirleir, Linda
(Administrative Promotor)
Seneca, Sara
(Co-Promotor)
Van Beeumen, Jozef
(Co-Promotor)
Van Coster, Rudy
(Co-Promotor)
Department of Embryology and Genetics
Pediatrics
Overview
Fingerprint
Research output
(1)
Activities
(10)
Research output
Research output per year
2009
2009
2009
1
Article
Research output per year
Research output per year
1 results
Publication Year, Title
(descending)
Publication Year, Title
(ascending)
Title
Type
Filter
Article
Search results
2009
Subcomplexes of mitochondrial complex V reveal mutations in mitochondrial DNA.
Smet, J.
,
Seneca, S.
,
De Paepe, B.
,
Meulemans, A.
,
Verhelst, H.
,
Leroy, J.
,
De Meirleir, L.
,
Lissens, W.
&
Vancoster, R.
,
Oct 2009
,
In:
Electrophoresis.
30
,
October
,
p. 3565-3572
8 p.
Research output
:
Contribution to journal
›
Article
›
peer-review
oligomycin sensitivity-conferring protein
100%
Mitochondrial DNA
65%
Mutation
52%
Native Polyacrylamide Gel Electrophoresis
22%
Oxidative Phosphorylation
17%
27
Citations (Scopus)