Thr1313Met Mutation in Skeletal Muscle Sodium Channels in a Japanese Family with Paramyotonia Congenita
スポンサーリンク
概要
- 論文の詳細を見る
- Japanese Society of Internal Medicineの論文
- 2003-09-01
著者
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Mitarai Tetsuya
Fourth Department Of Internal Medicine Saitama Medical Center Saitama Medical School
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KINOSHITA Masanobu
Fourth Department of Internal Medicine, Saitama Medical Center, Saitama Medical School
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SASAKI Ryogen
Department of Neurology, Mie University School of Medicine
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NAGANO Tadasuke
Fourth Department of Internal Medicine, Saitama Medical Center, Saitama Medical School
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MATSUDA Akihiko
the Fourth Department of Internal Medicine, Saitama Medical Center, Saitaina Medical School
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NAKAMURA Satoko
Fourth Department of Internal Medicine, Saitama Medical Center, Saitama Medical School
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TAKAHAMA Misato
Fourth Department of Internal Medicine, Saitama Medical Center, Saitama Medical School
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OHNUKI Manabu
Fourth Department of Internal Medicine, Saitama Medical Center, Saitama Medical School
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HASEGAWA Hajime
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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Nakamura Satoko
Fourth Department Of Internal Medicine Saitama Medical Center Saitama Medical School
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
- PLA2G6 variant in Parkinson's disease