Hereditary multiple cutaneous leiomyoma resulting from novel mutations in the fumarate hydratase gene
スポンサーリンク
概要
- 論文の詳細を見る
- 2008-08-01
著者
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Bladergroen Reno
Department Of Dermatology And Maastricht University Center For Molecular Dermatology (mucmd) Univers
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Jonkman Marcel
Department Of Dermatology University Medical Center Groningen University Of Groningen
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Jonkman Marcel
Department Of Dermatology Center For Blistering Diseases University Medical Center Groningen Univers
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Burrows Nigel
Department Of Dermatology Addenbrookes Hospital
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Van Steensel
Department Of Dermatology And Maastricht University Center For Molecular Dermatology (mucmd) Univers
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BADELOE Sadhanna
Department of Dermatology and Maastricht University Center for Molecular Dermatology (MUCMD), Univer
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STEIJLEN Peter
Department of Dermatology and Maastricht University Center for Molecular Dermatology (MUCMD), Univer
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POBLETE-GUTIERREZ Pamela
Department of Dermatology and Maastricht University Center for Molecular Dermatology (MUCMD), Univer
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VAN GEEL
Department of Dermatology and Maastricht University Center for Molecular Dermatology (MUCMD), Univer
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FRANK Jorge
Department of Dermatology and Maastricht University Center for Molecular Dermatology (MUCMD), Univer
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Van Geel
Department Of Dermatology And Maastricht University Center For Molecular Dermatology (mucmd) Univers
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Frank Jorge
Department Of Dermatology And Maastricht University Center For Molecular Dermatology (mucmd) Univers
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Steijlen Peter
Department Of Dermatology And Maastricht University Center For Molecular Dermatology (mucmd) Univers
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Poblete-gutierrez Pamela
Department Of Dermatology And Maastricht University Center For Molecular Dermatology (mucmd) Univers
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Badeloe Sadhanna
Department Of Dermatology And Maastricht University Center For Molecular Dermatology (mucmd) Univers
関連論文
- Two major 5'-untranslated regions for type XVII collagen mRNA
- Hereditary multiple cutaneous leiomyoma resulting from novel mutations in the fumarate hydratase gene
- Long-term follow-up of patients with recessive dystrophic epidermolysis bullosa in the Netherlands : Expansion of the mutation database and unusual phenotype-genotype correlations
- A recurrent mutation in variegate porphyria patients from Chile and Sweden : Evidence for a common genetic back-ground?
- Hereditary skin diseases of hemidesmosomes