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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

Detalles Bibliográficos
Autores principales: Naamane, H, Ailal, F, Abidi, O, Jeddane, L, Najib, J, Barakat, A, Bousfiha, AA
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3019518/
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author Naamane, H
Ailal, F
Abidi, O
Jeddane, L
Najib, J
Barakat, A
Bousfiha, AA
author_facet Naamane, H
Ailal, F
Abidi, O
Jeddane, L
Najib, J
Barakat, A
Bousfiha, AA
author_sort Naamane, H
collection PubMed
description
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institution National Center for Biotechnology Information
language English
publishDate 2011
publisher BioMed Central
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spelling pubmed-30195182011-01-13 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 Ailal, F Abidi, O Jeddane, L Najib, J Barakat, A Bousfiha, AA BMC Proc Poster Presentation BioMed Central 2011-01-10 /pmc/articles/PMC3019518/ Text en Copyright ©2011 Naamane et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Poster Presentation
Naamane, H
Ailal, F
Abidi, O
Jeddane, L
Najib, J
Barakat, A
Bousfiha, AA
The 752delG26 mutation in the RFXANK gene associated with major histocompatibility complex class II deficiency: evidence for a founder effect in the Moroccan population
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
title_full The 752delG26 mutation in the RFXANK gene associated with major histocompatibility complex class II deficiency: evidence for a founder effect in the Moroccan population
title_fullStr The 752delG26 mutation in the RFXANK gene associated with major histocompatibility complex class II deficiency: evidence for a founder effect in the Moroccan population
title_full_unstemmed The 752delG26 mutation in the RFXANK gene associated with major histocompatibility complex class II deficiency: evidence for a founder effect in the Moroccan population
title_short The 752delG26 mutation in the RFXANK gene associated with major histocompatibility complex class II deficiency: evidence for a founder effect in the Moroccan population
title_sort 752delg26 mutation in the rfxank gene associated with major histocompatibility complex class ii deficiency: evidence for a founder effect in the moroccan population
topic Poster Presentation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3019518/
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