Safety and immunogenicity of Fc‐EDA, a recombinant ectodysplasin A1 replacement protein, in human subjects

In X‐linked hypohidrotic ectodermal dysplasia, the most frequent ectodermal dysplasia, an inherited deficiency of the signalling protein ectodysplasin A1 (EDA1) impairs the development of the skin and its appendages, various eccrine glands, and dentition. The severe hypohidrosis common to X‐linked h...

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Detalles Bibliográficos
Autores principales: Körber, Iris, Klein, Ophir D., Morhart, Patrick, Faschingbauer, Florian, Grange, Dorothy K., Clarke, Angus, Bodemer, Christine, Maitz, Silvia, Huttner, Kenneth, Kirby, Neil, Durand, Caroline, Schneider, Holm
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7495278/
https://www.ncbi.nlm.nih.gov/pubmed/32250462
http://dx.doi.org/10.1111/bcp.14301

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7495278/
https://www.ncbi.nlm.nih.gov/pubmed/32250462
http://dx.doi.org/10.1111/bcp.14301

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