Rapid Determination of Chimerism Status Using Dihydrorhodamine Assay in a Patient with X-linked Chronic Granulomatous Disease Following Hematopoietic Stem Cell Transplantation

Chronic granulomatous disease (CGD) is a rare genetic disease, which is caused by defects in the NADPH oxidase complex (gp91(phox), p22(phox), p40(phox), p47(phox), and p67(phox)) of phagocytes. This defect results in impaired production of superoxide anions and other reactive oxygen species (ROS),...

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Detalles Bibliográficos
Autores principales: Kim, Hyun-Young, Kim, Hee-Jin, Ki, Chang-Seok, Kim, Dae Won, Yoo, Keon Hee, Kang, Eun-Suk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Laboratory Medicine 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3698309/
https://www.ncbi.nlm.nih.gov/pubmed/23826567
http://dx.doi.org/10.3343/alm.2013.33.4.288

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3698309/
https://www.ncbi.nlm.nih.gov/pubmed/23826567
http://dx.doi.org/10.3343/alm.2013.33.4.288

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