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

Research output: Contribution to journalLetter

3 Citations (Scopus)
88 Downloads (Pure)
Original languageEnglish
Pages (from-to)1292-1294
Number of pages4
JournalBritish Journal of Dermatology
Volume173
Issue number5
Early online date22 Aug 2015
DOIs
Publication statusPublished - 26 Nov 2015

Cite this

Pohler, E. ; Cunningham, F. ; Sandilands, A. ; Cole, C. ; Digby, S. ; McMillan, J. R. ; Aristodemou, S. ; McGrath, J. A. ; Smith, F. J. D. ; Mclean, W. H. I. ; Munro, C. S. ; Zamiri, M. / Novel autosomal dominant mutation in loricrin presenting as prominent ichthyosis. In: British Journal of Dermatology. 2015 ; Vol. 173, No. 5. pp. 1292-1294.
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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.",
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month = "11",
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Pohler, E, Cunningham, F, Sandilands, A, Cole, C, Digby, S, McMillan, JR, Aristodemou, S, McGrath, JA, Smith, FJD, Mclean, WHI, Munro, CS & Zamiri, M 2015, 'Novel autosomal dominant mutation in loricrin presenting as prominent ichthyosis', British Journal of Dermatology, vol. 173, no. 5, pp. 1292-1294. https://doi.org/10.1111/bjd.13895

Novel autosomal dominant mutation in loricrin presenting as prominent ichthyosis. / Pohler, E.; Cunningham, F. (Lead / Corresponding author); Sandilands, A.; Cole, C.; Digby, S.; McMillan, J. R.; Aristodemou, S.; McGrath, J. A.; Smith, F. J. D.; Mclean, W. H. I.; Munro, C. S.; Zamiri, M.

In: British Journal of Dermatology, Vol. 173, No. 5, 26.11.2015, p. 1292-1294.

Research output: Contribution to journalLetter

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

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U2 - 10.1111/bjd.13895

DO - 10.1111/bjd.13895

M3 - Letter

C2 - 25965869

VL - 173

SP - 1292

EP - 1294

JO - British Journal of Dermatology

JF - British Journal of Dermatology

SN - 0007-0963

IS - 5

ER -