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A Mutation in Para-Hydroxybenzoate-Polyprenyl Transferase (COQ2) Causes Primary Coenzyme Q10 Deficiency

✍ Scribed by Catarina Quinzii; Ali Naini; Leonardo Salviati; Eva Trevisson; Plácido Navas; Salvatore DiMauro; Michio Hirano

Book ID: 117854745
Publisher: American Society of Human Genetics
Year: 2006
Tongue: English
Weight: 288 KB
Volume: 78
Category: Article
ISSN: 0002-9297
DOI: 10.1086/500092

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