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Fatal infantile cardioencephalomyopathy with COX deficien... | ResearchHub
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Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene
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Authors
Lefkothea Papadopoulou
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Lefkothea Papadopoulou
•
Carolyn Sue
24 more
•
Eric Schon
Published
November 1, 1999
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Journal
Nature Genetics
Topics
Biology
Molecular Biology
Phenotype
Cytochrome C Oxidase
Mutation
Show all topics
DOI
10.1038/15513
