Compound heterozygosity for premature termination codon and glycine substitution mutations in the COL7A1 gene in Korean siblings with a moderately severe phenotype of recessive dystrophic epidermolysis bullosa
スポンサーリンク
概要
- 論文の詳細を見る
- 2003-12-01
著者
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Shimizu Hiroshi
Department of Bioinformatic Engineering, Graduate School of Information Science and Technology, Osak
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KIM Jooyoung
Department of Electrical and Electronic Engineering, Toyohashi University of Technology
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Kim Jooyoung
Department Of Dermatology And Cutaneous Biology Research Institute Yonsei University College Of Medi
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YASUKAWA Kana
Department of Dermatology, Hokkaido University Graduate School of Medicine
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KIM Soo-Chan
Department of Dermatology and Cutaneous Biology Research Institute, Yonsei University College of Med
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Kim Soo-chan
Department Of Dermatology And Cutaneous Biology Research Institute Yonsei University College Of Medi
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Shimizu Hiroshi
Department Of Bioinformatic Engineering Graduate School Of Information Science And Technology Osaka
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Yasukawa Kana
Department Of Dermatology And Clinical Research Institute National Sapporo Hospital
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Kim Soo-chan
Department Of Dermatology And Cutaneous Biology Research Institute Yonsei University College Of Medi
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Shimizu Hiroshi
Department Of Animal Science Faculty Of Agriculture Hokkaido University
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SHIMIZU HIROSHI
Department of Anatomy, School of Medicine, Tokushima University
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