mitochondria diary

ミトコンドリア病の治療法研究開発のための学術情報収集とシェア

薬物療法とヒト疾患に関連する乳酸アシドーシス

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C Zanza, V Facelli, T Romenskaya, M Bottinelli… - Pharmaceuticals, 2022
… to the mitochondrial matrix. These are genetical diseases and the genes that are
mutated are mainly connected to deficiency in the function of pyruvate
dehydrogenase (PDHA1) [60] or in a mitochondrial transfer RNA gene (MT-TL1) that …
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薬物療法とヒト疾患に関連する乳酸アシドーシス
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