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Chronic granulomatous disease in Morocco: genetic, immunological, and clinical features of 12 patients from 10 kindreds.
J Clin Immunol. 2014 May;34(4):452-8. doi: 10.1007/s10875-014-9997-3. Epub 2014 Mar 5.
J Clin Immunol. 2014.
PMID: 24596025
The 752delG26 mutation in the RFXANK gene associated with major histocompatibility complex class II deficiency: evidence for a founder effect in the Moroccan population.
Naamane H, El Maataoui O, Ailal F, Barakat A, Bennani S, Najib J, Hassar M, Saile R, Bousfiha AA.
Naamane H, et al. Among authors: el maataoui o.
Eur J Pediatr. 2010 Sep;169(9):1069-74. doi: 10.1007/s00431-010-1179-6. Epub 2010 Apr 23.
Eur J Pediatr. 2010.
PMID: 20414676
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