Clinical characteristics of a case of multiple mitochondrial dysfunction syndrome 3
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https://www.ncbi.nlm.nih.gov/bioproject/PRJNA971865
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资源简介：
To deepen the understanding of multiple mitochondrial dysfunction syndrome type 3 (MMDS3) caused by mutations in the IBA57 gene, we report a case of MMDS3 with onset of acute neurologic regression and review the literature.
创建时间：
2023-05-12
