Novel autosomal dominant mutation in loricrin presenting as prominent ichthyosis

E. Pohler; F. Cunningham; A. Sandilands; C. Cole; S. Digby; J. R. McMillan; S. Aristodemou; J. A. McGrath; F. J. D. Smith; W. H. I. Mclean; C. S. Munro; M. Zamiri

doi:10.1111/bjd.13895

Novel autosomal dominant mutation in loricrin presenting as prominent ichthyosis

E. Pohler, F. Cunningham (Lead / Corresponding author), A. Sandilands, C. Cole, S. Digby, J. R. McMillan, S. Aristodemou, J. A. McGrath, F. J. D. Smith, W. H. I. Mclean, C. S. Munro, M. Zamiri

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Original language	English
Pages (from-to)	1292-1294
Number of pages	4
Journal	British Journal of Dermatology
Volume	173
Issue number	5
Early online date	22 Aug 2015
DOIs	https://doi.org/10.1111/bjd.13895
Publication status	Published - 26 Nov 2015

ASJC Scopus subject areas

Dermatology

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10.1111/bjd.13895Licence: CC BY

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© 2015 The Authors. British Journal of Dermatology published by John Wiley & Sons Ltd on behalf of British Association of Dermatologists. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Final published version, 740 KBLicence: CC BY

Cite this

@article{18741c42709c4ac4a411ac09c4eea738,

title = "Novel autosomal dominant mutation in loricrin presenting as prominent ichthyosis",

author = "E. Pohler and F. Cunningham and A. Sandilands and C. Cole and S. Digby and McMillan, {J. R.} and S. Aristodemou and McGrath, {J. A.} and Smith, {F. J. D.} and Mclean, {W. H. I.} and Munro, {C. S.} and M. Zamiri",

note = "Funded by Wellcome Trust Strategic Award (Grant Number: 098439/Z/12/Z), Wellcome Trust Programme (Grant Number: 092530/Z/10/Z), Pachyonychia Congenita Project.",

year = "2015",

month = nov,

day = "26",

doi = "10.1111/bjd.13895",

language = "English",

volume = "173",

pages = "1292--1294",

journal = "British Journal of Dermatology",

issn = "0007-0963",

publisher = "Oxford University Press",

number = "5",

}

TY - JOUR

T1 - Novel autosomal dominant mutation in loricrin presenting as prominent ichthyosis

AU - Pohler, E.

AU - Cunningham, F.

AU - Sandilands, A.

AU - Cole, C.

AU - Digby, S.

AU - McMillan, J. R.

AU - Aristodemou, S.

AU - McGrath, J. A.

AU - Smith, F. J. D.

AU - Mclean, W. H. I.

AU - Munro, C. S.

AU - Zamiri, M.

N1 - Funded by Wellcome Trust Strategic Award (Grant Number: 098439/Z/12/Z), Wellcome Trust Programme (Grant Number: 092530/Z/10/Z), Pachyonychia Congenita Project.

PY - 2015/11/26

Y1 - 2015/11/26

UR - http://www.scopus.com/inward/record.url?scp=84939865188&partnerID=8YFLogxK

U2 - 10.1111/bjd.13895

DO - 10.1111/bjd.13895

M3 - Letter

C2 - 25965869

SN - 0007-0963

VL - 173

SP - 1292

EP - 1294

JO - British Journal of Dermatology

JF - British Journal of Dermatology

IS - 5

ER -

Novel autosomal dominant mutation in loricrin presenting as prominent ichthyosis

ASJC Scopus subject areas

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Other files and links

Dermatology and Genetic Medicine (Strategic Grant) (Joint with Kings College London)

Cite this

Novel autosomal dominant mutation in loricrin presenting as prominent ichthyosis

ASJC Scopus subject areas

Access to Document

Other files and links

Projects

Dermatology and Genetic Medicine (Strategic Grant) (Joint with Kings College London)

Cite this