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Complete human CD1a deficiency on Langerhans cells due to a rare point mutation in the coding sequence.
Complete human CD1a deficiency on Langerhans cells due to a rare point mutation in the coding sequence.
2016
Daniela Cerny
Duyen Huynh Thi Le
Roland Zuest
Kandhadayar Gopalan Srinivasan
Sumathy Velumani
Chiea Chuen Khor
Lucia Mori
Cameron P. Simmons
Michael Poidinger
Francesca Zolezzi
Florent Ginhoux
Muzlifah Haniffa
Bridget Wills
Katja Fink
Keywords:
Immunology
Biopsy
HEK 293 cells
HLA-DR Antigen
K562 cells
Antigen-presenting cell
Point mutation
Epidermis (botany)
Cell culture
Medicine
Correction
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