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:
Poster Presentation
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3019518/

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3019518/

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