Identification of defective Fas function and variation of the perforin gene in an epidermodysplasia verruciformis patient lacking EVER1 and EVER2 mutations [3]

Elisa Zavattaro; Barbara Azzimonti; Michele Mondini; Marco De Andrea; Cinzia Borgogna; Valentina Dell'Oste; Massimo Ferretti; Stefania Nicola; Giuseppe Cappellano; Adriana Carando; Giorgio Leigheb; Santo Landolfo; Umberto Dianzani; Marisa Gariglio

doi:10.1038/sj.jid.5701124

Identification of defective Fas function and variation of the perforin gene in an epidermodysplasia verruciformis patient lacking EVER1 and EVER2 mutations [3]

Elisa Zavattaro
, Barbara Azzimonti
, Michele Mondini
, Marco De Andrea
, Cinzia Borgogna
, Valentina Dell'Oste
, Massimo Ferretti
, Stefania Nicola
, Giuseppe Cappellano
, Adriana Carando
, Giorgio Leigheb
, Santo Landolfo
, Umberto Dianzani
, Marisa Gariglio

Research output: Contribution to journal › Letter › peer-review

Original language	English
Pages (from-to)	732-735
Number of pages	4
Journal	Journal of Investigative Dermatology
Volume	128
Issue number	3
DOIs	https://doi.org/10.1038/sj.jid.5701124
Publication status	Published - Mar 2008

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10.1038/sj.jid.5701124

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Zavattaro, E., Azzimonti, B., Mondini, M., De Andrea, M., Borgogna, C., Dell'Oste, V., Ferretti, M., Nicola, S., Cappellano, G., Carando, A., Leigheb, G., Landolfo, S., Dianzani, U., & Gariglio, M. (2008). Identification of defective Fas function and variation of the perforin gene in an epidermodysplasia verruciformis patient lacking EVER1 and EVER2 mutations [3]. Journal of Investigative Dermatology, 128(3), 732-735. https://doi.org/10.1038/sj.jid.5701124

@article{fa229536f5e54bde87a1060135359a68,

title = "Identification of defective Fas function and variation of the perforin gene in an epidermodysplasia verruciformis patient lacking EVER1 and EVER2 mutations [3]",

author = "Elisa Zavattaro and Barbara Azzimonti and Michele Mondini and \{De Andrea\}, Marco and Cinzia Borgogna and Valentina Dell'Oste and Massimo Ferretti and Stefania Nicola and Giuseppe Cappellano and Adriana Carando and Giorgio Leigheb and Santo Landolfo and Umberto Dianzani and Marisa Gariglio",

year = "2008",

month = mar,

doi = "10.1038/sj.jid.5701124",

language = "English",

volume = "128",

pages = "732--735",

journal = "Journal of Investigative Dermatology",

issn = "0022-202X",

publisher = "Elsevier B.V.",

number = "3",

}

Zavattaro, E , Azzimonti, B, Mondini, M, De Andrea, M, Borgogna, C, Dell'Oste, V, Ferretti, M, Nicola, S, Cappellano, G, Carando, A, Leigheb, G, Landolfo, S, Dianzani, U & Gariglio, M 2008, 'Identification of defective Fas function and variation of the perforin gene in an epidermodysplasia verruciformis patient lacking EVER1 and EVER2 mutations [3]', Journal of Investigative Dermatology, vol. 128, no. 3, pp. 732-735. https://doi.org/10.1038/sj.jid.5701124

Identification of defective Fas function and variation of the perforin gene in an epidermodysplasia verruciformis patient lacking EVER1 and EVER2 mutations [3]. / Zavattaro, Elisa ; Azzimonti, Barbara; Mondini, Michele et al.
In: Journal of Investigative Dermatology, Vol. 128, No. 3, 03.2008, p. 732-735.

Research output: Contribution to journal › Letter › peer-review

TY - JOUR

T1 - Identification of defective Fas function and variation of the perforin gene in an epidermodysplasia verruciformis patient lacking EVER1 and EVER2 mutations [3]

AU - Zavattaro, Elisa

AU - Azzimonti, Barbara

AU - Mondini, Michele

AU - De Andrea, Marco

AU - Borgogna, Cinzia

AU - Dell'Oste, Valentina

AU - Ferretti, Massimo

AU - Nicola, Stefania

AU - Cappellano, Giuseppe

AU - Carando, Adriana

AU - Leigheb, Giorgio

AU - Landolfo, Santo

AU - Dianzani, Umberto

AU - Gariglio, Marisa

PY - 2008/3

Y1 - 2008/3

UR - https://www.scopus.com/pages/publications/39149092678

U2 - 10.1038/sj.jid.5701124

DO - 10.1038/sj.jid.5701124

M3 - Letter

SN - 0022-202X

VL - 128

SP - 732

EP - 735

JO - Journal of Investigative Dermatology

JF - Journal of Investigative Dermatology

IS - 3

ER -

Identification of defective Fas function and variation of the perforin gene in an epidermodysplasia verruciformis patient lacking EVER1 and EVER2 mutations [3]

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