Complete human CD1a deficiency on Langerhans cells due to a rare point mutation in the coding sequence
Guardado en:
| Autor principal: | |
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| Formato: | Journal Article |
| Lenguaje: | inglés |
| Publicado: |
2018
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| Acceso en línea: | https://demo7.dspace.org/handle/123456789/100 |
| Etiquetas: |
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