High frequency of the risk allele of rs4132601 and rs11978267 from the IKZF1 gene in indigenous Mexican population

Author:

Gutiérrez‐Franco Jorge1,Ayón‐Pérez Miriam Fabiola2,Durán‐Avelar Ma. de Jesús2,Vibanco‐Pérez Norberto2,Sánchez‐Jasso Diego Eduardo2,Bañuelos‐Aguayo Dulce Guadalupe2,Sánchez‐Meza Jaime2,Pimentel‐Gutiérrez Helia Judith3,Zambrano‐Zaragoza José Francisco1,Agraz‐Cibrián Juan Manuel1,Vázquez‐Reyes Alejandro2ORCID

Affiliation:

1. Laboratorio de Inmunología Unidad Académica de Ciencias Químico‐Biológicas y Farmacéuticas Universidad Autónoma de Nayarit Tepic Nayarit México

2. Laboratorios de Investigación en Biología Molecular e Inmunología Unidad Académica de Ciencias Químico Biológicas y Farmacéuticas Universidad Autónoma de Nayarit Tepic Nayarit México

3. CharitéUniversitätsmedizin, Virchow‐Klinikum Berlin Germany

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Reference43 articles.

1. 1000Genomes‐study. (2019a).SNP‐rs4132601 U.S. National Library of Medicine. dbSNP Short Genetic Variations.https://www.ncbi.nlm.nih.gov/snp/rs4132601#frequency_tab

2. 1000Genomes‐study. (2019b).SNP‐rs11978267 U.S. National Library of Medicine. dbSNP Short Genetic Variations.https://www.ncbi.nlm.nih.gov/snp/rs11978267

3. World Medical Association Declaration of Helsinki: ethical principles for medical research involving human subjects;Association, G. A. o. t. W. M.;The Journal of the American College of Dentists,2014

4. IKZF1 gene polymorphisms increased the risk of childhood acute lymphoblastic leukemia in an Iranian population

5. Prognostic value of rare IKZF1 deletion in childhood B-cell precursor acute lymphoblastic leukemia: an international collaborative study

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