Multisystem involvement in Chinese patients with neuromyopathic phenotype of mitochondrial trifunctional protein deficiency

二维码有效期 120s

作者 Wei Cui-Jie ^[1] Chang Xing-Zhi ^[1] Ge Lin ^[1] Fu Xiao-Na ^[1] Fan Yan-Bin ^[1] Liu Jie-Yu ^[1] Wang Shuang ^[1] Li Hai-Li ^[2] Yang Yan-Ling ^[1] Xiong Hui ^[1] 学术成果认领

作者单位 Department of Pediatrics, Peking University First Hospital, Beijing 100034, China ^[1] Department of Ophthalmology, Peking University First Hospital, Beijing 100034, China ^[2]

栏目名称 Clinical Observation

DOI 10.1097/CM9.0000000000000805

发布时间 2025-03-04

基金项目

This work was supported by grants from the National Key Research and Development Program of China the National Natural Science Foundation of China the Beijing Key Laboratory of Molecular Diagnosis and Study on Pediatric Genetic Diseases This work was supported by grants from the National Key Research and Development Program of China the National Natural Science Foundation of China the Beijing Key Laboratory of Molecular Diagnosis and Study on Pediatric Genetic Diseases

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中华医学杂志英文版

2020年133卷11期

1358-1360页

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Multisystem involvement in Chinese patients with neuromyopathic phenotype of mitochondrial trifunctional protein deficiency

Multisystem involvement in Chinese patients with neuromyopathic phenotype of mitochondrial trifunctional protein deficiency

中华医学杂志英文版

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中华医学杂志英文版

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Multisystem involvement in Chinese patients with neuromyopathic phenotype of mitochondrial trifunctional protein deficiency

Multisystem involvement in Chinese patients with neuromyopathic phenotype of mitochondrial trifunctional protein deficiency

中华医学杂志英文版

相似文献

中华医学杂志英文版

相关期刊

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