Mild phenotypes and proper supercomplex assembly in human cells carrying the homoplasmic m.15557G > A mutation in cytochrome b gene.

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Mild phenotypes and proper supercomplex assembly in human cells carrying the homoplasmic m.15557G > A mutation in cytochrome b gene.

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2017 nî lūn-bûn

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Mild phenotypes and proper sup ...... mutation in cytochrome b gene.

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Mild phenotypes and proper sup ...... mutation in cytochrome b gene.

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Mild phenotypes and proper sup ...... mutation in cytochrome b gene.

@en

Mild phenotypes and proper sup ...... mutation in cytochrome b gene.

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Mild phenotypes and proper sup ...... mutation in cytochrome b gene.

@en

Mild phenotypes and proper sup ...... mutation in cytochrome b gene.

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P1476

Mild phenotypes and proper sup ...... mutation in cytochrome b gene.

@en

P2093

Anna Ghelli

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Anna Maria Porcelli

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Concetta Valentina Tropeano

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Giulia Leone

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Giuseppe Gasparre

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Ivana Kurelac

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Laura Benedetta Amato

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P2860

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Structure and function of cytochrome bc complexes.

The molecular evolution of the Qo motif

Identification of ubiquinol binding motifs at the Qo-site of the cytochrome bc1 complex

Mammalian pyrimidine biosynthesis: fresh insights into an ancient pathway.

Proton-coupled electron transfer at the Qo-site of the bc1 complex controls the rate of ubihydroquinone oxidation.

Mitochondrial Disease-related Mutation G167P in Cytochrome b of Rhodobacter capsulatus Cytochrome bc1 (S151P in Human) Affects the Equilibrium Distribution of [2Fe-2S] Cluster and Generation of Superoxide.

The cytochrome b p.278Y>C mutation causative of a multisystem disorder enhances superoxide production and alters supramolecular interactions of respiratory chain complexes.

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92-102

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scholarly article

P356

10.1002/HUMU.23350

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P433

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P478

http://www.w3.org/2001/XMLSchema#string

P50

Luisa Iommarini

P577

2017-10-01T00:00:00Z

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P698

28967163

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