Please use this identifier to cite or link to this item:
http://www.edream.ma:8080/jspui/handle/123456789/2328| Title: | The 752delG26 mutation in the RFXANK gene associated with major histocompatibility complex class II deficiency: Evidence for a founder effect in the Moroccan population |
| Authors: | Naamane, Hamid El Maataoui, Ouafaa Ailal, Fatima Barakat, Abdelhamid Bennani, Siham Najib, Jilali Hassar, Mohammed Saile, Rachid Bousfiha, Ahmed Aziz |
| Keywords: | MHC class II immunodeficiency RFXANK gene Molecular diagnosis Founder effect Morocco |
| Issue Date: | 2010 |
| Publisher: | European Journal of Pediatrics |
| URI: | http://dream:8080/jspui/handle/123456789/2328 |
| Appears in Collections: | Medicine, Research & Experimental |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| The 752delG26 mutation in the RFXANK gene associated with major histocompatibility complex class II deficiency Evidence for a founder effect in the Moroccan population.pdf | 248.72 kB | Adobe PDF | View/Open |
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