Sequence analysis of nuclear genes encoding functionally important complex I subunits in children with encephalomyopathy.
about
The p.M292T NDUFS2 mutation causes complex I-deficient Leigh syndrome in multiple familiesDown-regulation of mitochondrial acyl carrier protein in mammalian cells compromises protein lipoylation and respiratory complex I and results in cell death.Genetic aetiology of ophthalmological manifestations in children - a focus on mitochondrial disease-related symptoms.Nodularia spumigena extract induces upregulation of mitochondrial respiratory chain complexes in spinach (Spinacia oleracea L.)
P2860
Sequence analysis of nuclear genes encoding functionally important complex I subunits in children with encephalomyopathy.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
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2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
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2005年學術文章
@zh-hant
name
Sequence analysis of nuclear g ...... ildren with encephalomyopathy.
@en
Sequence analysis of nuclear g ...... ildren with encephalomyopathy.
@nl
type
label
Sequence analysis of nuclear g ...... ildren with encephalomyopathy.
@en
Sequence analysis of nuclear g ...... ildren with encephalomyopathy.
@nl
prefLabel
Sequence analysis of nuclear g ...... ildren with encephalomyopathy.
@en
Sequence analysis of nuclear g ...... ildren with encephalomyopathy.
@nl
P2093
P2860
P1476
Sequence analysis of nuclear g ...... hildren with encephalomyopathy
@en
P2093
Anne M Remes
Heikki Rantala
Ilmo E Hassinen
Johanna Uusimaa
Kari Majamaa
P2860
P2888
P304
P356
10.1007/S00109-005-0712-Y
P577
2005-09-03T00:00:00Z