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Susanne Schwonbeck
Susanne Schwonbeck
Biology
Mutation
Dermatology
Missense mutation
Acral peeling skin syndrome
2
Papers
48
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A Missense Mutation in TGM5 Causes Acral Peeling Skin Syndrome in a Tunisian Family
2009
Journal of Investigative Dermatology
M. Kharfi
Nadia El Fekih
Donia Ammar
Habib Jaafoura
Susanne Schwonbeck
Maurice A.M. van Steensel
Bécima Fazaa
Mohamed Ridha Kamoun
Judith Fischer
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Citations (28)
An Autosomal-Recessive Form of Cutis Laxa Is Due to Homozygous Elastin Mutations, and the Phenotype May Be Modified by a Heterozygous Fibulin 5 Polymorphism
2009
Journal of Investigative Dermatology
Hala Mégarbané
Jobard Florence
Jörn Oliver Sass
Susanne Schwonbeck
Mario Foglio
Rafael de Cid
Susan Cure
Safa Saker
André Mégarbané
Judith Fischer
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Citations (20)
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