A hypermorphic IκBα mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency
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author: Christine Chable-Bessia Rainer Doffinger Françoise Le Deist Caterina Cancrini Asma Smahi Alain Israel Arnold Munnich Jean-Laurent Casanova Christine Bodemer Paolo Rossi Anne Puel Francesco Novelli Janine Reichenbach Jacqueline Feinberg |
| Publication date | October 1, 2003 |
| Language | English |
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