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The 752delG26 mutation in theRFXANKgene associated with major histocompatibility complex class II deficiency: evidence for a founder effect in the Moroccan population

✍ Scribed by Hamid Naamane; Ouafaa El Maataoui; Fatima Ailal; Abdelhamid Barakat; Siham Bennani; Jilali Najib; Mohammed Hassar; Rachid Saile; Ahmed Aziz Bousfiha

Publisher: Springer
Year: 2010
Tongue: English
Weight: 249 KB
Volume: 169
Category: Article
ISSN: 0340-6997
DOI: 10.1007/s00431-010-1179-6

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