(Q56941191)

English

A hypermorphic IκBα mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency

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A hypermorphic IκBα mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency (English)
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Gilles Courtois
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Rainer Döffinger
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Marion Bonnet
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Shoji Yamaoka
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Sophie Dupuis-Girod
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Susanna Livadiotti
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Alain Fischer
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Alain Israël
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1 October 2003
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112
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1108-1115
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7
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