A Patient with Myotonic Dystrophy Type 1 (DM1) Accompanied by Laryngeal and Renal Cell Carcinomas Had a Small CTG Triplet Repeat Expansion But No Somatic Instability in Normal Tissues
スポンサーリンク
概要
著者
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Mitarai Tetsuya
Fourth Department Of Internal Medicine Saitama Medical Center Saitama Medical School
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HIROSE Kazuhiko
Ueno Hospital Internal Medicine
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KINOSHITA Masanobu
the Fourth Department of Internal Medicine, Saitama Medical Center, Saitama Medical School
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OSANAI Ryuichi
the Department of Otolaryngology, Saitama Medical Center, Saitama Medical School
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KIKKAWA Masaru
the Foruth Department of Internal Medicine, Saitama Medical Center, Satiama Medical School
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ADACHI Akiko
the Department of Pathology, Saitama Medical Center, Saitama Medical School
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OHTAKE Toshiyuki
the Department of Neurolog, Tokyo Metropolitan Neurological Hopspital
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KOMORI Tetsuo
the Department of Neurolog, Tokyo Metropolitan Neurological Hopspital
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HASHIMOTO Kohzo
Toyobo Gene Analysis Co. LTD
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ITOYAMA Shinnji
the Department of Pathology, Saitama Medical Center, Saitama Medical School
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MITARAI Tetsuya
the Foruth Department of Internal Medicine, Saitama Medical Center, Satiama Medical School
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Adachi Akiko
The Department Of Pathology Saitama Medical Center Saitama Medical School
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Komori Tetsuo
The Department Of Neurolog Tokyo Metropolitan Neurological Hopspital
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Osanai Ryuichi
The Department Of Otolaryngology Saitama Medical Center Saitama Medical School
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Kikkawa Masaru
The Foruth Department Of Internal Medicine Saitama Medical Center Satiama Medical School
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Hashimoto Kohzo
Toyobo Gene Analysis
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Itoyama Shinnji
The Department Of Pathology Saitama Medical Center Saitama Medical School
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Mitarai Tetsuya
The Foruth Department Of Internal Medicine Saitama Medical Center Satiama Medical School
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Kinoshita Masanobu
The Fourth Department Of Internal Medicine Saitama Medical Center Saitama Medical School
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Ohtake Toshiyuki
The Department Of Neurolog Tokyo Metropolitan Neurological Hopspital
関連論文
- Adrenomedullin Amidation Enzyme Activities in Hypertensive Patients
- Thr1313Met Mutation in Skeletal Muscle Sodium Channels in a Japanese Family with Paramyotonia Congenita
- A Patient with Myotonic Dystrophy Type 1 (DM1) Accompanied by Laryngeal and Renal Cell Carcinomas Had a Small CTG Triplet Repeat Expansion But No Somatic Instability in Normal Tissues
- Eradication of Helicobacter pylori Restores Elevation of Serum Gastrin Concentrations in Patients with End-Stage Renal Disease
- Thr1313Met Mutation in Skeletal Muscle Sodium Channels in a Japanese Family with Paramyotonia Congenita
- Evaluation of Fungal DNA Sequence Using Polymerase Chain Reaction in Infection-free Vitreous Humor
- An Autopsy Case of Light Chain Deposition Disease.
- A Case of Congenital Dyserythropoietic Anemia Type II Associated with Hemochromatosis.