Author:
Sandilands Aileen,Terron-Kwiatkowski Ana,Hull Peter R,O'Regan Gráinne M,Clayton Timothy H,Watson Rosemarie M,Carrick Thomas,Evans Alan T,Liao Haihui,Zhao Yiwei,Campbell Linda E,Schmuth Matthias,Gruber Robert,Janecke Andreas R,Elias Peter M,van Steensel Maurice A M,Nagtzaam Ivo,van Geel Michel,Steijlen Peter M,Munro Colin S,Bradley Daniel G,Palmer Colin N A,Smith Frances J D,McLean W H Irwin,Irvine Alan D
Publisher
Springer Science and Business Media LLC
Reference24 articles.
1. Smith, F.J.D. et al. Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris. Nat. Genet. 38, 337–342 (2006).
2. Palmer, C.N.A. et al. Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis. Nat. Genet. 38, 441–446 (2006).
3. Judge, M.R., McLean, W.H.I. & Munro, C.S. Disorders of keratinization. in Rook's Textbook of Dermatology Vol. 2 (eds. Burns, T., Breathnach, S., Cox, C. & Griffiths, C.) 34.54–34.56 (Blackwell Scientific, Oxford, 2004).
4. Sandilands, A. et al. Prevalent and rare mutations in the gene encoding filaggrin cause ichthyosis vulgaris and predispose individuals to atopic dermatitis. J. Invest. Dermatol. 126, 1770–1775 (2006).
5. Gruber, R. et al. Filaggrin mutations p.R501X and c.2282del4 in ichthyosis vulgaris. Eur. J. Hum. Genet. 15, 179–184 (2007).
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