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). (Q45328418)
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scientific article published on 28 June 2013
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | 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). |
scientific article published on 28 June 2013 |
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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). (English)
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Emmanuel Scalais
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Ronit Chafai
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Rudy Van Coster
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Lutz Bindl
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Christian Nuttin
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Chryssa Panagiotaraki
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Sara Seneca
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Willy Lissens
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Antonia Ribes
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Caroline Geers
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Linda De Meirleir
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28 June 2013
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17
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6
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625-630
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