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Meneka K. Sidhu
Meneka K. Sidhu
UCL Institute of Neurology
Medicine
Epilepsy
Mitochondrial disease
Mitochondrial DNA
Progressive myoclonus epilepsy
3
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1
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Progressive myoclonic epilepsy due to rare mitochondrial ND6 mutation, m.14487T>C.
2021
Anthony Khoo
Saadnah Naidu
Surapi Bhairavi Wijayendran
Ashirwad Merve
Fion Bremner
Meneka K. Sidhu
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Late diagnoses of Dravet syndrome: How many individuals are we missing?
2021
Katri Silvennoinen
Clinda Puvirajasinghe
Kirsty Hudgell
Meneka K. Sidhu
Helena Martins Custodio
Wendy D Jones
Simona Balestrini
Sanjay M. Sisodiya
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