(Q55784996)
English
neonatal severe cardiopulmonary failure due to mitochondrial methylation defect
human disease
- Combined Oxidative Phosphorylation Deficiency type 28
- Combined oxidative phosphorylation defect type 28
- COXPD28
- Combined Oxidative Phosphorylation Deficiency 28
- combined oxidative phosphorylation deficiency 28
Statements
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Identifiers
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