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Muneerah M. Alsubaie

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Identifying NDUFA12 mutation in a Saudi family: An unusual presentation of mitochondrial Complex I deficiency mimicking as idiopathic intracranial hypertension in a patient with papilledema and visual loss

Journal of Family and Community Medicine Q2 2026 10.4103/jfcm.jfcm_322_25

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Journal of Family and Community Medicine

🇸🇦 Q2 AMS 88

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