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Early myoclonic epilepsy, hypertrophic cardiomyopathy and subsequently a nephrotic syndrome in a patient with CoQ10 deficiency caused by mutations in para-hydroxybenzoate-polyprenyl transferase (COQ2) by Scalais, Emmanuel; Chafai, Ronit; Van Coster, Rudy; Bindl, Lutz; Nuttin, Christian; Panagiotaraki, Chryssa; Seneca, Sara; Lissens, Willy; Ribes, Antonia; Geers, Caroline; Smet, Joel; De Meirleir, Linda is a Medicine article available to read on EtoBox.

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Author
Scalais, Emmanuel; Chafai, Ronit; Van Coster, Rudy; Bindl, Lutz; Nuttin, Christian; Panagiotaraki, Chryssa; Seneca, Sara; Lissens, Willy; Ribes, Antonia; Geers, Caroline; Smet, Joel; De Meirleir, Linda
Publisher
Elsevier Science; Elsevier ; W. B. Saunders Co., Ltd.; Elsevier BV (ISSN 1090-3798)
Published
2013
Field
Medicine (Health Sciences)