Sumita Ryo | Tonami General Hospital
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概要
関連著者
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Terai Hidenobu
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Ino Hidekazu
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Hayashi Kenshi
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Shimizu Masami
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Yamaguchi Masato
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Mabuchi Hiroshi
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Shimizu Masami
Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Graduate School O
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Terai Hidenobu
Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Graduate School O
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Sumita Ryo
Tonami General Hospital
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Itoh Hideki
Department Of Emergency And Critical Care Medicine Kanazawa University Hospital
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Mabuchi Hiroshi
Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Graduate School O
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Yamaguchi Masato
Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Graduate School O
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Uchiyama Katsuharu
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Konno Tetsuo
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Hayashi Tatsumi
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Sakata Kenji
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Inoue Masaru
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Inoue Masaru
Division Of Cardiology Ishikawa Prefectural Hospital
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Mabuchi Tomohito
Department of Cardiology, Fukui Prefectural Hospital
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Higashida Haruhiro
Department Of Biophysical Genetics Kanazawa University Graduate School Of Medical Science
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Uchiyama Katsuharu
Division Of Cardiovascular Medicine Kanazawa University Graduate School Of Medical Science
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Sakata Kenji
金沢大学 医学系研究科循環器内科学
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Higashida Haruhiro
Biophysical Genetics, Division of Neuroscience, Kanazawa University Graduate School of Medical Scien
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Kaneda Tomoya
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Kaneda Tomoya
Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Graduate School O
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Kiyama Masaru
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Mabuchi Tomohito
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Sakazume Shinobu
Division of Pediatrics, NHO Kanazawa Medical Center
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Mabuchi Tomohito
Department Of Cardiology Fukui Prefectural Hospital
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Ohosato Kazuo
Fukui Cardiovascular Center
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Ohe Kotaro
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
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Hayashi Tatsumi
Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Kanazawa Universi
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Oe Kotaro
Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Graduate School O
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Ohe Koutarou
Fukui Cardiovascular Center
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Higasida Haruhiro
Department Of Biophysical Genetics Kanazawa Universty Graduate School Of Medical Science
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Kametani Tomio
Department Of Internal Medicine Koseiren Takaoka Hospital
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Sakazume Shinobu
Angiogenesis and Vascular Developement, Division of Cardiovascular Medicine, Graduate School of Medi
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Haraki Tatsuo
Department Of Internal Medicine Komatsu Municipal Hospital
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Mabuchi Tomohito
Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Graduate School O
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Sakazume Shinobu
Division Of Pediatrics Nho Kanazawa Medical Center
著作論文
- Double Missense Mutations (D611Y in KCNQ1 and D609G in HERG) in a Japanese Family with Long QT Syndrome
- Novel KCNQ1 missense mutation (D611Y) in a Japanese long QT family