Biochemical Assessment of Coenzyme Q10 Deficiency.

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Coenzyme Q10 Supplementation in Aging and Disease.Biochemical Assessment and Monitoring of Mitochondrial Disease.Perturbed Redox Signaling Exacerbates a Mitochondrial Myopathy

P2860

Q49829630-E1D9AC2E-8A73-4D66-8304-182AD2501D28 Q55005075-244AC3DB-6ED7-4AD1-B1EA-1C002CD5809C Q58696816-461B81FA-F206-4312-A0FD-F5C64D6BE839

P2860

Biochemical Assessment of Coenzyme Q10 Deficiency.

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http://www.wikidata.org/entity/Q39168844

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2017 nî lūn-bûn

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2017年の論文

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2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

2017年论文

@zh

2017年论文

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name

Biochemical Assessment of Coenzyme Q10 Deficiency.

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Biochemical Assessment of Coenzyme Q10 Deficiency.

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Biochemical Assessment of Coenzyme Q10 Deficiency.

@en

Biochemical Assessment of Coenzyme Q10 Deficiency.

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Biochemical Assessment of Coenzyme Q10 Deficiency.

@en

Biochemical Assessment of Coenzyme Q10 Deficiency.

@nl

P1476

Biochemical Assessment of Coenzyme Q10 Deficiency.

@en

P2093

Ana Belén Cortés

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

Daniel J M Fernández-Ayala

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

Juan Carlos Rodríguez-Aguilera

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

Plácido Navas

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P2860

The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene

Mitochondrial COQ9 is a lipid-binding protein that associates with COQ7 to enable coenzyme Q biosynthesis

Mitochondrial ADCK3 employs an atypical protein kinase-like fold to enable coenzyme Q biosynthesis

A mutation in para-hydroxybenzoate-polyprenyl transferase (COQ2) causes primary coenzyme Q10 deficiency

COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness.

A nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial disease

CABC1 gene mutations cause ubiquinone deficiency with cerebellar ataxia and seizures

ADCK3, an ancestral kinase, is mutated in a form of recessive ataxia associated with coenzyme Q10 deficiency

Prenyldiphosphate synthase, subunit 1 (PDSS1) and OH-benzoate polyprenyltransferase (COQ2) mutations in ubiquinone deficiency and oxidative phosphorylation disorders

Cerebellar Ataxia and Coenzyme Q Deficiency through Loss of Unorthodox Kinase Activity

P31

scholarly article

P356

10.3390/JCM6030027

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

P433

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

P478

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

P577

2017-03-05T00:00:00Z

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

P698

28273876

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

P921

ubidecarenone

P932

5372996

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

Biochemical Assessment of Coenzyme Q10 Deficiency.

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P2860

P2860

Biochemical Assessment of Coenzyme Q10 Deficiency.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P31

P356

P433

P478

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P31

P356

P433

P478

P577

P698

P921

P932