The 752delG26 mutation in the RFXANK gene associated with...

BMC Proceedings 2011 / 12 Vol. 5; Iss. 1 Suppleme

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

H Naamane, F Ailal, O Abidi, L Jeddane, J Najib, A Barakat, AA Bousfiha
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Volume:
5
Language:
english
Pages:
1
DOI:
10.1186/1753-6561-5-s1-p88
Date:
December, 2011
File:
PDF, 173 KB
english, 2011
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