Three novelHBBmutations, c.-140C>G (-90 C>G), c.237_256delGGACAACCTCAAGGGCACCT (FS Cd 78/85 -20 bp), and c.315+2T>G (IVS2:2 T>G). Update of the mutational spectrum of β-Thalassemia in Mexican mestizo patients-Reference-Cited by-同舟云学术

Three novelHBBmutations, c.-140C>G (-90 C>G), c.237_256delGGACAACCTCAAGGGCACCT (FS Cd 78/85 -20 bp), and c.315+2T>G (IVS2:2 T>G). Update of the mutational spectrum of β-Thalassemia in Mexican mestizo patients

Published:2017-06-12 Issue:5 Volume:39 Page:539-545
ISSN:1751-5521
Container-title:International Journal of Laboratory Hematology
language:en
Short-container-title:Int J Lab Hem

Author:

Rizo-de-la-Torre L. C.¹²,Ibarra B.¹,Sánchez-López J. Y.²,Magaña-Torres M. T.²,Rentería-López V. M.²,Perea-Díaz F. J.²^ORCID

Affiliation:

1. Doctorado en Genética Humana, Centro Universitario de Ciencias de la Salud; Universidad de Guadalajara; Guadalajara Jalisco México

2. División de Genética, Centro de Investigación Biomédica de Occidente; Instituto Mexicano del Seguro Social; Guadalajara Jalisco México

Funder

Fondo de Investigación en Salud

Publisher

Wiley

Subject

Biochemistry (medical),Clinical Biochemistry,Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ijlh.12692/fullpdf

Reference41 articles.

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2. World distribution, population genetics, and health burden of the hemoglobinopathies;Williams;Cold Spring Harb Perspect Med,2012

3. The population genetics of the haemoglobinopathies;Flint;Baillieres Clin Haematol,1998

4. The Molecular Basis of β Thalassemia, δβ Thalassemia, and Hereditary Persistence of Fetal Hemoglobin

5. Molecular spectrum of β-thalassemia in the Mexican population;Perea;Blood Cells Mol Dis,2004

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