Mutation spectrum of MMACHC in Chinese patients with combined methylmalonic aciduria and homocystinuria
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概要
- 論文の詳細を見る
- Nature Publishing Groupの論文
- 2010-09-01
著者
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Hsiao K‐j
National Yang‐ming Univ. Taipei Twn
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QI Yu
Central Lab, Peking University First Hospital
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Qi Yu
Peking University First Hospital
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Lin Shuan-pei
Department Of Pediatrics Mackay Memorial Hospital
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HSIAO Kwang-Jen
Institute of Genetics, National Yang-Ming University
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Yang Yan-ling
Department Of Hepatobiliary Surgery Xijing Hospital Fourth Military Medical University
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Qi Y
Department Of Pediatrics Peking University First Hospital
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CHIU Yen-Hui
Institute of Genetics, National Yang-Ming University
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LIU Tze-Tze
Department of Education and Research, Taipei City Hospital
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Chang Ying-chen
Genome Research Center National Yang-ming University
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Lin Shuan-pei
Departments Of Pediatrics And Medical Research Mackay Memorial Hospital And Mackay Medicine Nursing And Management College
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LIU Mei-Ying
Institute of Genetics, National Yang-Ming University
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CHIANG Szu-Hui
Department of Medical Research and Education, Taipei Veterans General Hospital
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HAN Lian-Shu
Department of Pediatric Endocrinology and Genetic Metabolism, Shanghai Institute for Pediatric Research, Xinhua Hospital, Shanghai Jiaotong University School of Medicine
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HSIAO Kwang-Jen
Department of Medical Research and Education, Taipei Veterans General Hospital
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LIU Tze-Tze
Genome Research Center, National Yang-Ming University
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Liu Mei-ying
Institute Of Genetics National Yang-ming University
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Han Lian-shu
Department Of Pediatric Endocrinology And Genetic Metabolism Shanghai Institute For Pediatric Research Xinhua Hospital Shanghai Jiaotong University School Of Medicine
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Chiang Szu-hui
Department Of Medical Research And Education Taipei Veterans General Hospital
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Liu Tze-tze
Department Of Education And Research Taipei City Hospital
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- Analysis of SCN1A mutation and parental origin in patients with Dravet syndrome
- Mutation spectrum of MMACHC in Chinese patients with combined methylmalonic aciduria and homocystinuria
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