Inherited Keratinocyte Diseases (Ichthyosis and Related Disorders)
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Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-540-78814-0_50
Reference50 articles.
1. Smith FJ, Irvine AD, Terron-Kwiatkowski A et al (2006) Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris. Nat Genet 38:337–342
2. Palmer CNA, Irvine AD, Terron-Kwiatkowski A et al (2006) Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis. Nat Genet 38:441–446
3. Scott IR, Harding CR, Barrett JG (1982) Histidine-rich protein of the keratohyalin granules. Sourse of the free amino acids, urocanic acid and pyrrolidone carboxylic acid in the stratum corneum. Biochimica Biophysica Acta 719:110–117
4. Hernandez-Martin A, Gonzalez-Sarmiento R, De Unamuno P (1999) X-linked ichthyosis: an update. Br J Dermatol 141:617–627
5. Elias PM, Crumrine D, Rassner U et al (2004) Basis for abnormal desquamation and permeability barrier dysfunction in RXLI. J Invest Dermatol 122:314–319
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