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A Mutation in Para-Hydroxybenzoate-Polyprenyl Transferase... | ResearchHub
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A Mutation in Para-Hydroxybenzoate-Polyprenyl Transferase (COQ2) Causes Primary Coenzyme Q10 Deficiency
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Authors
Catarina Quinzii
6 more
Catarina Quinzii
•
Ali Naini
4 more
•
Michio Hirano
Published
January 6, 2006
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Journal
The American Journal of Human Genetics
Topics
Biology
Biochemistry
Molecular Biology
Electrical And Electronic Engineering
Mutation
Show all topics
DOI
10.1086/500092
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publisher-specific-oa
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Journal
The American Journal of Human Genetics
Topics
Biology
Biochemistry
Molecular Biology
Electrical And Electronic Engineering
Mutation
Show all topics
DOI
10.1086/500092
License
publisher-specific-oa
