An attempt to analyze the pathogenesis of congenital keratinization disorders, and the future prospects of gene therapy for the patients in our out-patient department
Author:
Affiliation:
1. Department of Dermatology, Juntendo University School of Medicine
Publisher
The Jutendo Medical Journal
Link
https://www.jstage.jst.go.jp/article/pjmj/49/1/49_24/_pdf
Reference29 articles.
1. 1) HardmanMJ, SisiP, BanburyDN, et al.: Patterned acquisition of skin barrier function during development. Development, 1998; 125: 1541-1552.
2. 2) RoopD: Defects in the barrier. Science, 1995; 267: 474-475.
3. 3) OgawaH, HattoriM, IshibashiY: Abnormal fibrous protein isolated from the stratum corneum of a patient with bullous congenital ichthyosiform erythroderma ( BCIE ). Arch Dermatol Res., 1979; 266: 109-116.
4. 4) RothnagelJA, DomineyAM, DempseyLD, et al.: Mutations in the rod domains of keratins 1 and 10 in epidermolytic hyperkeratosis. Science, 1992; 257: 1128-1130.
5. 5) SugaY, DuncanKO, HealdPW, et al.: A novel helix termination mutation in keratin 10 in annular epidermolytic ichthyosis, a variant of bullous congenital ichthyosiform erythroderma. J Invest Dermatol, 1998; 111: 1220-1223.
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