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Severe macrophage activation syndrome. Is there a causative role for a homozygous A91V mutation in the perforin gene?

Detalles Bibliográficos
Autores principales:	Girschick, H, Rossi, R, Kölsch, U, Ammann, S, Lohse, P, Morbach, H, von Bernuth, H, Ehl, S
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2015
Materias:	Poster Presentation
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4597326/ http://dx.doi.org/10.1186/1546-0096-13-S1-P20

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