ArticleBMJ neurology open2021
Progressive myoclonic epilepsy due to rare mitochondrial ND6 mutation, m.14487T>C.
Anthony Khoo et al.PubMed ↗Full text ↗Publisher ↗
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ArticleBMJ neurology open2021
Anthony Khoo et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.