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Volumn 52, Issue 4, 2000, Pages 392-394
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Severe neonatal mitochondrial cytopathy due to isolated COX defects;Citopatía mitocondrial neonatal grave por déficit aislado de COX
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(Spain)
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Author keywords
Cytochrome c oxidase; Mitochondria; Mitochondrial cytopathy; Neonate
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Indexed keywords
CYTOCHROME C OXIDASE;
LACTIC ACID;
MITOCHONDRIAL DNA;
PYRUVIC ACID;
ARTICLE;
BRAIN DISEASE;
CARDIOMYOPATHY;
CASE REPORT;
CAUSE OF DEATH;
ENZYME DEFECT;
GENETIC COUNSELING;
HEART INFARCTION;
HEART MUSCLE ISCHEMIA;
HISTOLOGY;
HUMAN;
HUMAN TISSUE;
NEWBORN;
PHENOTYPE;
CYTOCHROME-C OXIDASE DEFICIENCY;
HUMANS;
INFANT, NEWBORN;
MALE;
MITOCHONDRIAL MYOPATHIES;
SEVERITY OF ILLNESS INDEX;
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EID: 0034449326
PISSN: 03024342
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (1)
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References (14)
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