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The 752delG26 Mutation in the RFXANK Gene Associated With Major Histocompatibility Complex Class II Deficiency: Evidence for a Founder Effect in the Moroccan Population
BMC Proceedings
- United Kingdom
doi 10.1186/1753-6561-5-s1-p88
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Categories
Biochemistry
Medicine
Genetics
Molecular Biology
Date
January 10, 2011
Authors
H Naamane
F Ailal
O Abidi
L Jeddane
J Najib
A Barakat
AA Bousfiha
Publisher
Springer Science and Business Media LLC
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