Sporadic Congenital Hyperthyroidism due to a Germline Mutation in the Thyrotropin Receptor Gene (Leu 512 Gln) in a Japanese Patient
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概要
- 論文の詳細を見る
- 2006-12-01
著者
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Miyauchi A
Kuma Hospital
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Yamauchi Akira
Kuma Hospital
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Ito Mitsuru
Kuma Hospital
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Katsu K
Second Department Of Internal Medicine Osaka Medical College
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MIYAUCHI Akira
Kuma Hospital
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KUMA Kanji
Kuma Hospital
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HISHINUMA Akira
Department of Clinical Laboratory Medicine, Dokkyo University School of Medicine
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Ohe H
First Department Of Internal Medicine Kagawa Medical University
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Amino N
Kuma Hospital
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Amino Nobuyuki
Department Of Laboratory Medicine Osaka University Graduate School Of Medicine
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Amino Nobuyuki
Departments Of Laboratory Medicine Osaka University Medical School
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Amino Nobuyuki
Kuma Hospital
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FUKATA Shuji
Kuma Hospital
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Nishihara Eijun
Kuma Hospital
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Nishihara Eijun
The First Department Of Internal Medicine Nagasaki University School Of Medicine
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KUBOTA SUMIHISA
Kuma Hospital
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KUDO TAKUMI
Kuma Hospital
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OHYE HIDEMI
Kuma Hospital
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Ito Mitsura
First Department Of Medicine Osaka Medical College
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Miyauchi Akira
Lightwave Transmission Engineering Department Fujitsu Limited
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Kojima Keishi
The Second Department Of Internal Medicine Osaka Medical College
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Kojima Keishi
Second Department Of Internal Medicine Osaka Medical College
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Hishinuma Akira
Department Of Clinical Laboratory Medicine Dokkyo University School Of Medicine
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Hishinuma Akira
Department Of Clinical Laboratory Medicine Dokkyo Medical University
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Kuma Kanji
Department Of Surgery Kuma Hospital
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