Molecular analysis of afibrinogenemic mutations caused by a homozygous FGA1238 bp deletion, and a compound heterozygous FGA1238 bp deletion and novel FGA c.54+3A>C substitution
スポンサーリンク
概要
- 論文の詳細を見る
- 2012-07-01
著者
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Terasawa Fumiko
Shinshu Univ. Jpn
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Terasawa Fumiko
Department Of Biomedical Laboratory Sciences School Of Health Sciences Shinshu University
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Okumura Nobuo
Shinshu Univ. Jpn
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OKUMURA Nobuo
Department of Biomedical Laboratory Sciences, School of Health Sciences, Shinshu University
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Fujiwara Mitsuhiro
Department Of Pediatrics And Department Of Hematology/oncology Kurashiki Central Hospital
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Sugano Mitsutoshi
Department Of Laboratory Medicine Shinshu University School Of Medicine
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Matsuda Kazuyuki
Department Of Internal Medicine Yamaguchi Prefecture General Hospital
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TAKEZAWA Yuka
Department of Health and Medical Sciences, Graduate School of Medicine, Shinshu University
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TANAKA Aiko
Department of Pediatrics, Kurashiki Central Hospital
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KAINUMA Keigo
Department of Pediatrics, Mie Prefectural Medical Center Hospital
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Takezawa Yuka
Department Of Health And Medical Sciences Graduate School Of Medicine Shinshu University
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Kainuma Keigo
Department Of Pediatrics Mie Prefectural Medical Center Hospital
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Okumura Nobuo
Department Of Health And Medical Sciences Graduate School Of Medicine Shinshu University
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Tanaka Aiko
Department Of Pediatrics Kurashiki Central Hospital
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Okumura Nobuo
Department Of Biomedical Laboratory Sciences School Of Health Sciences Shinshu University
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Sugano Mitsutoshi
Department Of Laboratory Medicine Shinshu University Hospital
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MATSUDA Kazuyuki
Department of Laboratory Medicine, Shinshu University Hospital
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Tanaka Aiko
Department of Medicine, Shiga University of Medical Science
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