Genetic analysis of a severe case of Netherton syndrome and application for prenatal testing

Netherton syndrome (NS) is a rare autosomal recessive disease with variable expression. It is defined by a triad of symptoms: congenital ichthyosiform erythroderma, trichorrhexis invaginata and atopy. Recently, genetic linkage has been established to the SPINK5 gene locus on chromosome 5q32 encoding...

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Hauptverfasser: Müller, F. B. (VerfasserIn) , Haußer-Siller, Ingrid (VerfasserIn) , Berg, D. (VerfasserIn) , Casper, C. (VerfasserIn) , Maiwald, R. (VerfasserIn) , Jung, A. (VerfasserIn) , Jung, H. (VerfasserIn) , Korge, Bernhard P. (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 20 April 2002
In: British journal of dermatology
Year: 2002, Jahrgang: 146, Heft: 3, Pages: 495-499
ISSN:1365-2133
DOI:https://doi.org/10.1046/j.1365-2133.2002.04625.x
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/https://doi.org/10.1046/j.1365-2133.2002.04625.x
Verlag, lizenzpflichtig, Volltext: https://www.onlinelibrary.wiley.com/doi/abs/10.1046/j.1365-2133.2002.04625.x
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Verfasserangaben:F.B. Müller, I. Haußer, D. Berg, C. Casper, R. Maiwald, A. Jung, H. Jung and B.P. Korge

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