Genetic basis for iMCD-TAFRO

TAFRO syndrome, a clinical subtype of idiopathic multicentric Castleman disease (iMCD), consists of a constellation of symptoms/signs including thrombocytopenia, anasarca, fever, reticulin fibrosis/renal dysfunction, and organomegaly. The etiology of iMCD-TAFRO and the basis for cytokine hypersecret...

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Publicado en:Oncogene
Main Authors: Yoshimi, Akihide, Trippett, Tanya M., Zhang, Nan, Chen, Xueyan, Penson, Alexander V., Arcila, Maria E., Pichardo, Janine, Baik, Jeeyeon, Sigler, Allison, Harada, Hironori, Fajgenbaum, David, Dogan, Ahmet, Abdel-Wahab, Omar, Xiao, Wenbin
Formato: Artigo
Idioma:Inglês
Publicado: 2020
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Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC7148173/
https://ncbi.nlm.nih.gov/pubmed/32051554
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41388-020-1204-9
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