IPEX Syndrome with Normal FOXP3 Protein Expression in Treg Cells in an Infant Presenting with Intractable Diarrhea as a Single Symptom

Ali Al Maawali, Beata Derfalvi, Johan Van Limbergen, Andrew Issekutz, Thomas Issekutz, Hasan Ghandourah, Mohsin Rashid

Medicine

Producción científica: Contribución a una revista › Artículo › revisión exhaustiva

5 Citas (Scopus)

Huella

Profundice en los temas de investigación de 'IPEX Syndrome with Normal FOXP3 Protein Expression in Treg Cells in an Infant Presenting with Intractable Diarrhea as a Single Symptom'. En conjunto forman una huella única.

Medicine & Life Sciences