Prevalence and clinical prediction of mitochondrial disorders in a large neuropediatric cohort
Neurological symptoms are frequent and often a leading feature of childhood‐onset mitochondrial disorders (MD) but the exact incidence of MD in unselected neuropediatric patients is unknown. Their early detection is desirable due to a potentially rapid clinical decline and the availability of manage...
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Veröffentlicht in: | Clinical genetics 2021-12, Vol.100 (6), p.766-770 |
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Hauptverfasser: | , , , , , , , , , , , , , , , , , |
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Sprache: | eng |
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