Compound heterozygous PMP22 deletion mutations causing severe Charcot-Marie-Tooth disease type 1
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概要
- 論文の詳細を見る
- 2010-11-01
著者
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Hayasaka K
Department Of Pediatrics Yamagata University School Of Medicine
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Hayasaka Kiyoshi
Department Of Pediatrics Yamagata University Faculty Of Medicine
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NUMAKURA CHIKAHIKO
Department of Pediatrics, Yamagata University School of Medicine
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Shirahata Emi
Department Of Pediatrics Yamagata University School Of Medicine
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Shirahata Emi
Department Of Pediatrics Yamagata City Hospital Saiseikan
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Numakura C
Department Of Pediatrics Yamagata University School Of Medicine
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Numakura Chikahiko
Department Of Pediatrics Yamagata University School Of Medicine
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Nakamura Kazuyuki
Department Of Biochemistry And Biomolecular Recognition Yamaguchi University School Of Medicine
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Kato Mitsuhiro
Department Of Applied Chemistry Aichi Institute Of Technology
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KISHIKAWA Yumiko
Department of Pediatrics, Yamagata University School of Medicine
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Kishikawa Yumiko
Department Of Pediatrics Yamagata University School Of Medicine
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ABE Akiko
Department of Pediatrics, Yamagata University School of Medicine
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Abe Akiko
Department Of Pediatrics Yamagata University School Of Medicine
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Seiwa Chizuru
Department Of Pediatrics Yamagata Medical Rehabilitation Center For Disabled Persons
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HONMA Tomomi
Department of Pediatrics, Yamagata Prefectural Shinjo Hospital
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ITOH Aiko
Department of Pediatrics, Yamagata Medical Rehabilitation Center for Disabled Persons
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Honma Tomomi
Department Of Pediatrics Yamagata Prefectural Shinjo Hospital
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Itoh Aiko
Department Of Pediatrics Yamagata Medical Rehabilitation Center For Disabled Persons
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Nakamura Kazuyuki
Department Of Pediatrics Yamagata University School Of Medicine
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ABE Akiko
Department of Obstetrics and Gynecology, The University of Tokushima, School of Medicine
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ABE AKIKO
Department of Gerodontology, School of Dentistry, Aichi Gakuin University
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