Mitochondrial cardioencephalopathy due to a COQ4 mutation.

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Mitochondrial cardioencephalopathy due to a COQ4 mutation.

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http://www.wikidata.org/entity/Q41015269

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2017 nî lūn-bûn

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2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

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@zh-tw

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2017年论文

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Mitochondrial cardioencephalopathy due to a COQ4 mutation.

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Item

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Mitochondrial cardioencephalopathy due to a COQ4 mutation.

@en

prefLabel

Mitochondrial cardioencephalopathy due to a COQ4 mutation.

@en

P1476

Mitochondrial cardioencephalopathy due to a COQ4 mutation

@en

P2093

Josef Finsterer

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

P2860

Renal manifestations of primary mitochondrial disorders.

Novel recessive mutations in COQ4 cause severe infantile cardiomyopathy and encephalopathy associated with CoQ10 deficiency.

Coenzyme Q 10 improves lactic acidosis, strokelike episodes, and epilepsy in a patient with MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes).

Isolated mitochondrial myopathy associated with muscle coenzyme Q10 deficiency.

Effects of antiepileptic drugs on mitochondrial functions, morphology, kinetics, biogenesis, and survival.

P304

7-8

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P31

scholarly article

P356

10.1016/J.YMGMR.2017.07.003

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P478

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

P50

Sinda Zarrouk Mahjoub

P577

2017-07-13T00:00:00Z

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P698

28736720

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P932

5510520

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

Mitochondrial cardioencephalopathy due to a COQ4 mutation.

about

Mitochondrial cardioencephalopathy due to a COQ4 mutation.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P50

P577

P698

P932