20th World Congress of Dermatology
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SY0990
On the pathogenesis of alopecia areata
P0705
A mutation in connexin 31 is associated with recessive erythrokeratodermia variabilis (EKV) and leads to defective membranous localization


1st TO 5th JULY 2002
PARIS



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Foreword

Oral communications and co-opted speakers abstracts

Poster abstracts

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