Complete human CD1a deficiency on Langerhans cells due to a rare point mutation in the coding sequence
Uložené v:
| Hlavný autor: | |
|---|---|
| Médium: | Journal Article |
| Jazyk: | English |
| Vydavateľské údaje: |
2018
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| On-line prístup: | https://demo7.dspace.org/handle/123456789/100 |
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