Transglutaminase 1 replacement therapy successfully mitigates the autosomal recessive congenital ichthyosis phenotype in full-thickness skin disease equivalents.

Item Type:	Letter
Title:	Transglutaminase 1 replacement therapy successfully mitigates the autosomal recessive congenital ichthyosis phenotype in full-thickness skin disease equivalents.
Creators Name:	Plank, R. and Yealland, G. and Miceli, E. and Lima Cunha, D. and Graff, P. and Thomforde, S. and Gruber, R. and Moosbrugger-Martinz, V. and Eckl, K. and Calderón, M. and Hennies, H.C. and Hedtrich, S.
Keywords:	Topical Administration, Needle Biopsy, Recessive Genes, Genetic Predisposition to Disease, Lamellar Ichthyosis, Immunohistochemistry, Mutation, Prognosis, Sampling Studies, Transglutaminases, Treatment Outcome
Source:	Journal of Investigative Dermatology
ISSN:	0022-202X
Publisher:	Elsevier
Volume:	139
Number:	5
Page Range:	1191-1195
Date:	May 2019
Official Publication:	https://doi.org/10.1016/j.jid.2018.11.002
PubMed:	View item in PubMed

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