Suchergebnisse - "Fushimi, Takuya"

PubPharm (2)

1

Mitochondrial ribosomal protein PTCD3 mutations cause oxidative phosphorylation defects with Leigh syndrome

enthalten in: Neurogenetics | 2019

von Borna, N. | Kishita, Y. | Kohda, M. | +12

2

Clinical validity of biochemical and molecular analysis in diagnosing Leigh syndrome: a study of 106 Japanese patients

enthalten in: Journal of inherited metabolic disease | 2017

von Ogawa, E. | Shimura, M. | Fushimi, T. | +14

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