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Novel mutations in MTERF3: First report of a new genetic cause in two Chinese patients with developmental delay, intermittent hypoglycemia and metabolic acidosis.
Duan R, Mahlatsi RL, Wang Y, Xu C, Wang M, Zou Z, Liu Z, Jiang H, Duan X, Deng J, Song M, Liu Y, Fang H, Lyu J, Fang F. Duan R, et al. Among authors: wang y, wang m. Mitochondrion. 2025 Jun 19;85:102059. doi: 10.1016/j.mito.2025.102059. Online ahead of print. Mitochondrion. 2025. PMID: 40543543 Free article.
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