Publication:
Novel mutation of the electron transferring flavoprotein dehydrogenase (ETFDH) gene in the isolated myopathic form of coenzyme q10 deficiency

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Date

2015-01-01

Authors

Authors

Görükmez, O.
Görükmez, Orhan
Sağ, Şebnem Özemri
Erdöl, Şahin
Sağlam, Halil
Yakut, T.

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Medecine Et Hygiene

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Keywords

Q(10) deficiency, Mitochondrial encephalomyopathy, Science & technology, Life sciences & biomedicine, Biotechnology & applied microbiology, Genetics & heredity, Medical ethics, Medicine, research & experimental, Biotechnology & applied microbiology, Genetics & heredity, Medical ethics, Research & experimental medicine

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