PLACK syndrome shows remarkable phenotypic homogeneity
- 2 October 2018
- journal article
- editorial
- Published by Oxford University Press (OUP) in Clinical and Experimental Dermatology
- Vol. 44 (5) , 580-583
Abstract
No abstract availableFunding Information
- Ram family
This publication has 5 references indexed in Scilit:
- Filaggrin 2 Deficiency Results in Abnormal Cell-Cell Adhesion in the Cornified Cell Layers and Causes Peeling Skin Syndrome Type AJournal of Investigative Dermatology, 2018
- PLACK syndrome resulting from a new homozygous insertion mutation in CASTJournal of Dermatological Science, 2017
- Calpain 12 Function Revealed through the Study of an Atypical Case of Autosomal Recessive Congenital IchthyosisJournal of Investigative Dermatology, 2017
- Loss-of-Function Mutations in CAST Cause Peeling Skin, Leukonychia, Acral Punctate Keratoses, Cheilitis, and Knuckle PadsThe American Journal of Human Genetics, 2015
- Peeling off the genetics of atopic dermatitis–like congenital disordersJournal of Allergy and Clinical Immunology, 2014