A point mutation in the protein 4.2 gene (allele 4.2 Tozeur) associated with hereditary haemolytic anaemia

Author:

Hayette S.,Morle L.,Bozon M.,Ghanem A.,Risinger M.,Korsgren C.,Tanner M. J. A.,Fattoum S.,Cohen C. M.,Delaunay J.

Publisher

Wiley

Subject

Hematology

Reference47 articles.

1. Band 3 Coimbra: a variant associated with dominant hereditary spherocytosis and band 3 deficiency. (Abstract);Alloisio;Blood,1993

2. Elliptocytogenic α1/36 spectrin Sfax lacks 9 amino acids in helix 3 of repeat 4: evidence for the activation of a cryptic 5'-splice site in exon 8 of spectrin α-gene;Baklouti;Blood,1992

3. Protein 4.2mRNA splicing isoforms are tissue specific and regulated during erythroid differentiation. (Abstract);Bouhassira;Blood,1990

4. An alanine-to-threonine substitution in protein 4.2 cDNA is associated with a Japanese form of hereditary hemolytic anemia (protein 4.2NIPPON);Bouhassira;Blood,1992

5. Human erythrocyte membrane protein band 4.2 (pallidin);Cohen;Seminars in Hematology,1993

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