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1دورية أكاديميةCongenital ichthyosiform erythroderma with epidermolysis due to a novel frameshift mutation in KRT10
المؤلفون: Bernadett Kurz, MD, Kevin-Thomas Koschitzki, MD, Ute Hehr, MD, Ute Germer, MD, Julia Schreml, MD, Florian Langhammer, MD, Stephan Schreml, MD
المصدر: JAAD Case Reports, Vol 35, Iss , Pp 74-76 (2023)
مصطلحات موضوعية: congenital ichthyosiform erythroderma, filaggrin (FLG) gene, keratin 10 (KRT10) gene, keratinopathic ichthyoses, Dermatology, RL1-803
وصف الملف: electronic resource
العلاقة: http://www.sciencedirect.com/science/article/pii/S2352512623000929Test; https://doaj.org/toc/2352-5126Test
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2Congenital ichthyosiform erythroderma with epidermolysis due to a novel frameshift mutation in KRT10
المؤلفون: Kurz, Bernadett, Koschitzki, Kevin-Thomas, Hehr, Ute, Germer, Ute, Schreml, Julia, Langhammer, Florian, Schreml, Stephan
المصدر: JAAD Case Rep
مصطلحات موضوعية: ddc:610, congenital ichthyosiform erythroderma filaggrin (FLG) gene keratin 10 (KRT10) gene keratinopathic ichthyoses, 610 Medizin, Case Report, Dermatology
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1216784e3bc428b074613551269bca02Test