A recurrent mutation in variegate porphyria patients from Chile and Sweden : Evidence for a common genetic back-ground?
スポンサーリンク
概要
- 論文の詳細を見る
- 2011-01-01
著者
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Harper Pauline
Porphyria Centre Sweden C2-71 Department Of Medical Laboratory Sciences And Technology Division Of C
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Bladergroen Reno
Department Of Dermatology And Maastricht University Center For Molecular Dermatology (mucmd) Univers
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Floderus Ylva
Porphyria Centre Sweden C2-71 Department Of Medical Laboratory Sciences And Technology Division Of C
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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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Poblete-gutierrez Pamela
Department Of Dermatology And Maastricht University Center For Molecular Dermatology (mucmd) Univers
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Ernst Manon
Department Of Dermatology Maastricht University Medical Centre (mumc)
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VAN SEROOSKERKEN
Department of Dermatology, Maastricht University Medical Centre (MUMC)
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WOLFF Carlos
Departamento de Medicina Occidente, Universidad de Chile
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Wolff Carlos
Departamento De Medicina Occidente Universidad De Chile
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Van Serooskerken
Department Of Dermatology Maastricht University Medical Centre (mumc)
関連論文
- Novel mutations and phenotypic effect of the splice site modulator IVS3-48C in nine Swedish families with erythropoietic protoporphyria
- Two novel mutations and coexistence of the 991C>T and the 1339C>T mutation on a single allele in the coproporphyrinogen oxidase gene in Swedish patients with hereditary coproporphyria
- Hereditary multiple cutaneous leiomyoma resulting from novel mutations in the fumarate hydratase gene
- A recurrent mutation in variegate porphyria patients from Chile and Sweden : Evidence for a common genetic back-ground?