COA6 基因新发变异致婴儿细胞色素c 氧化酶缺陷致心脑肌病4 型 1 例报告并文献复习
崔清洋,尚云,曹银利，等
Infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency- 4 caused by a novel mutation of COA6 gene: a case report and literature review
CUI Qingyang, SHANG Yun, CAO Yinli, et al
临床儿科杂志
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2021, (4): 251
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DOI: 10.3969/j.issn.1000-3606.2021.04.003
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