Clinical, biochemical and molecular analyses of six patients with isolated cytochrome c oxidase deficiency due to mutations in the SCO2 gene.
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Tissue-specific cytochrome c oxidase assembly defects due to mutations in SCO2 and SURF1Biochemical diagnosis of mitochondrial disordersNoninvasive diagnostics of mitochondrial disorders in isolated lymphocytes with high resolution respirometryAnalysis of mouse models of cytochrome c oxidase deficiency owing to mutations in Sco2Mitochondrial cardioencephalomyopathy due to a novel SCO2 mutation in a Brazilian patient: case report and literature review.Central nervous system manifestations of mitochondrial disorders.Role of SCOX in determination of Drosophila melanogaster lifespanIsolated cytochrome c oxidase deficiency in G93A SOD1 mice overexpressing CCS proteinThe mitochondrion: a central architect of copper homeostasis.
P2860
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P2860
Clinical, biochemical and molecular analyses of six patients with isolated cytochrome c oxidase deficiency due to mutations in the SCO2 gene.
description
2004 nî lūn-bûn
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2004年の論文
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2004年学术文章
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name
Clinical, biochemical and mole ...... to mutations in the SCO2 gene.
@en
Clinical, biochemical and mole ...... to mutations in the SCO2 gene.
@nl
type
label
Clinical, biochemical and mole ...... to mutations in the SCO2 gene.
@en
Clinical, biochemical and mole ...... to mutations in the SCO2 gene.
@nl
prefLabel
Clinical, biochemical and mole ...... to mutations in the SCO2 gene.
@en
Clinical, biochemical and mole ...... to mutations in the SCO2 gene.
@nl
P2093
P50
P1433
P1476
Clinical, biochemical and mole ...... to mutations in the SCO2 gene
@en
P2093
P304
P356
10.1080/08035250410008761
P407
P577
2004-10-01T00:00:00Z