Normal and abnormal mechanisms of gene splicing and relevance to inherited skin diseases
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概要
- 論文の詳細を見る
- 2005-11-01
著者
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MCGRATH John
Genetic Skin Disease Group, St. John's Institute of Dermatology, Division of Genetics and Molecular
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Mcgrath John
Genetic Skin Disease Group And The Robin Eady National Diagnostic Epidermolysis Bullosa Research Lab
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Mcgrath John
Genetic Skin Disease Group St. John's Institute Of Dermatology The Guy's King's Colle
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WESSAGOWIT Vesarat
Genetic Skin Disease Group and The Robin Eady National Diagnostic Epidermolysis Bullosa Research Lab
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NALLA Vijay
Laboratory of Human Molecular Genetics, Children's Mercy Hospitals and Clinics, University of Missou
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ROGAN Peter
Laboratory of Human Molecular Genetics, Children's Mercy Hospitals and Clinics, University of Missou
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Nalla Vijay
Laboratory Of Human Molecular Genetics Children's Mercy Hospitals And Clinics University Of Mis
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Rogan Peter
Laboratory Of Human Molecular Genetics Children's Mercy Hospitals And Clinics University Of Mis
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Wessagowit Vesarat
Genetic Skin Disease Group St. John's Institute Of Dermatology The Guy's King's Colle
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- Single nucleotide polymorphism in a commonly utilized LAMB3 primer sequence : Implications for mutation detection and haplotype analysis in junctional epidermolysis bullosa
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- Molecular Basis of Lipoid Proteinosis in Two Indian Siblings
- Focal dermal hypoplasia resulting from a new nonsense mutation, p. E300X, in the PORCN gene
- Human hair abnormalities resulting from inherited desmosome gene mutations
- Three-dimensional imaging reveals major changes in skin microvasculature in lipoid proteinosis and lichen sclerosus
- Normal and abnormal mechanisms of gene splicing and relevance to inherited skin diseases