Recessive epidermolytic hyperkeratosis caused by a previously unreported termination codon mutation in the keratin 10 gene

Patrick Terheyden; Gundula Grimberg; Ingrid Hausser; Christian Rose; Bernhard P. Korge; Thomas Krieg; Meral J. Arin

doi:10.1038/jid.2009.131

Recessive epidermolytic hyperkeratosis caused by a previously unreported termination codon mutation in the keratin 10 gene

Patrick Terheyden^*, Gundula Grimberg, Ingrid Hausser, Christian Rose, Bernhard P. Korge, Thomas Krieg, Meral J. Arin

^*Corresponding author for this work

Clinic of Dermatology, Allergology and Venerology

18 Citations (Scopus)

Original language	English
Journal	Journal of Investigative Dermatology
Volume	129
Issue number	11
Pages (from-to)	2721-2723
Number of pages	3
ISSN	0022-202X
DOIs	https://doi.org/10.1038/jid.2009.131
Publication status	Published - 11.2009

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10.1038/jid.2009.131

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title = "Recessive epidermolytic hyperkeratosis caused by a previously unreported termination codon mutation in the keratin 10 gene",

author = "Patrick Terheyden and Gundula Grimberg and Ingrid Hausser and Christian Rose and Korge, \{Bernhard P.\} and Thomas Krieg and Arin, \{Meral J.\}",

year = "2009",

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doi = "10.1038/jid.2009.131",

language = "English",

volume = "129",

pages = "2721--2723",

journal = "Journal of Investigative Dermatology",

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T1 - Recessive epidermolytic hyperkeratosis caused by a previously unreported termination codon mutation in the keratin 10 gene

AU - Terheyden, Patrick

AU - Grimberg, Gundula

AU - Hausser, Ingrid

AU - Rose, Christian

AU - Korge, Bernhard P.

AU - Krieg, Thomas

AU - Arin, Meral J.

PY - 2009/11

Y1 - 2009/11

UR - https://www.scopus.com/pages/publications/70350055357

U2 - 10.1038/jid.2009.131

DO - 10.1038/jid.2009.131

M3 - Letters

C2 - 19474805

AN - SCOPUS:70350055357

SN - 0022-202X

VL - 129

SP - 2721

EP - 2723

JO - Journal of Investigative Dermatology

JF - Journal of Investigative Dermatology

IS - 11

ER -

Recessive epidermolytic hyperkeratosis caused by a previously unreported termination codon mutation in the keratin 10 gene

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