Diagnosis of Japanese patients with HHH syndrome by molecular genetic analysis : a common mutation, R179X
スポンサーリンク
概要
- 論文の詳細を見る
- 2001-05-01
著者
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KANAZAWA Naomi
Department of Inherited Metabolic Disease, National Institute of Neuroscience, NCNP
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TSUJINO Seiichi
Department of Inherited Metabolic Disease, National Institute of Neuroscience, NCNP
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MIYAMOTO Takeshi
Department of Inherited Metabolic Disease, National Institute of Neuroscience, NCNP
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KATO Shigeo
Department of Internal Medicine, Shinfuji Hospital
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KAWAKAMI Masato
Department of Neurology, St. Marianna University School of Medicine
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INOUE Yoshito
Biochemical Section, Division of Human Genetics, Medical Research Institute, Kanazawa Medical Univer
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KUHARA Tomiko
Biochemical Section, Division of Human Genetics, Medical Research Institute, Kanazawa Medical Univer
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INOUE Takehiko
The Department of Pediatrics, Western Shimane Medical and Welfare Center for the Handicapped
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TAKESHITA Kenzo
Division of Child Neurology, Institute of Neurological Sciences, Faculty of Medicine, Tottori Univer
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Kanazawa Naomi
奈良県立医科大学 小児科学
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Kanazawa N
National Center Of Neurology And Psychiatry Tokyo Jpn
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Kanazawa Naomi
Department Of Inherited Metabolic Disease National Institute Of Neuroscience National Center Of Neur
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Miyamoto Takeshi
Department Of Cell Differentiation Sakaguchi Laboratory Of Developmental Biology Keio University Sch
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Takeshita Kenzo
Division Of Child Neurological Institute Of Neurology Sciences Faculty Of Medicine Tottori Universit
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Kato Shigeo
Department Of Astrophysics Nagoya University
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Inoue Yoshito
Biochemical Section Division Of Human Genetics Medical Research Institute Kanazawa Medical Universit
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Kuhara Tomiko
Biochemical Section Division Of Human Genetics Medical Research Institute Kanazawa Medical Universit
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Tsujino S
Department Of Inherited Metabolic Disease National Institute Of Neuroscience National Center Of Neur
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Tsujino Seiichi
Department Of Inherited Metabolic Disease National Institute Of Neuroscience National Center Of Neur
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Kawakami Masato
Department Of Neurology St. Marianna University School Of Medicine
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Kawakami Masato
Department Of Chemical And Biochemical Engineering Ariake National College Of Technology
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Takeshita Kenzo
Division Of Child Neurology Institute Of Neurological Sciences Faculty Of Medicine Tottori Universit
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Kato Shigeo
Department Of Internal Medicine Shinfuji Hospital
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Inoue Takehiko
The Department Of Pediatrics Western Shimane Medical And Welfare Center For The Handicapped
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Miyamoto Takeshi
Department Of Inherited Metabolic Disease National Institute Of Neuroscience Ncnp
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- Diagnosis of Japanese patients with HHH syndrome by molecular genetic analysis : a common mutation, R179X
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