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Megumi Saito-Tsuruoka

Saitama Medical University

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Author Correction: Prenatal diagnosis of severe mitochondrial diseases caused by nuclear gene defects: a study in Japan.

2021 Scientific Reports
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A Japanese family with P102L Gerstmann–Sträussler–Scheinker disease with a variant Creutzfeldt-Jakob disease-like phenotype among the siblings: A case report

2021 eNeurologicalSci
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Prenatal diagnosis of severe mitochondrial diseases caused by nuclear gene defects: a study in Japan.

2021 Scientific Reports
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