Analysis of the SLC4A1 gene in three Mexican patients with hereditary spherocytosis: report of a novel mutation-Reference-Cited by-同舟云学术

Analysis of the SLC4A1 gene in three Mexican patients with hereditary spherocytosis: report of a novel mutation

Published:2009-12-18 Issue:1 Volume:33 Page:9-11
ISSN:1678-4685
Container-title:Genetics and Molecular Biology
language:
Short-container-title:Genet. Mol. Biol.

Author:

Sánchez-López Josefina Y.¹,Camacho-Torres Ana L.¹,Ibarra Bertha²,Tintos Jesús A.²,Perea Francisco J.¹

Affiliation:

1. Instituto Mexicano del Seguro Social, Mexico

2. Instituto Mexicano del Seguro Social, Mexico; Universidad de Guadalajara, Mexico

Publisher

FapUNIFESP (SciELO)

Subject

Genetics,Molecular Biology

Link

http://www.scielo.br/pdf/gmb/v33n1/2009-244.pdf

Reference22 articles.

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2. A novel DI*A allele without the Band 3 Memphis mutation in Amazonian Indians;Baleotti W;Vox Sang,2003

3. Band 3 Memphis variant II. Altered stilbene disulfonate binding and the Diego (Dia) blood group antigen are associated with the human erythrocyte band 3 mutation Pro854 -> Leu;Bruce LJ;J Biol Chem,1994

4. Familial distal renal tubular acidosis is associated with mutations in the red cell anion exchanger (Band 3, AE1) gene;Bruce LJ;J Clin Invest,1997

5. Polymorphism analysis of G199A, Ncol in ANK1 and Memphis I in SLC4A1 genes in Mexican healthy individuals and subjects affected with hereditary spherocytosis;Camacho-Torres AL;Gac Méd Méx,2006

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