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

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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., Yealland, G., Miceli, E., Lima Cunha, D., Graff, P., Thomforde, S., Gruber, R., Moosbrugger-Martinz, V., Eckl, K., Calderón, M., 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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