β-Spectrin Promissão: A Translation Initiation Codon Mutation of the β-Spectrin Gene (ATG → GTG) Associated With Hereditary Spherocytosis and Spectrin Deficiency in a Brazilian Family-Reference-Cited by-同舟云学术

β-Spectrin Promissão: A Translation Initiation Codon Mutation of the β-Spectrin Gene (ATG → GTG) Associated With Hereditary Spherocytosis and Spectrin Deficiency in a Brazilian Family

Published:1998-01-01 Issue:1 Volume:91 Page:368-369
ISSN:1528-0020
Container-title:Blood
language:en
Short-container-title:

Author:

Bassères Daniela S.¹,Vicentim Dilmara L.¹,Costa Fernando F.¹,Saad Sara T.O.¹,Hassoun Hani²

Affiliation:

1. Hemocentro Universidade Estadual de Campinas, Brazil

2. Division of Hematology/Oncology St Elizabeth's Medical Center, Boston, MA

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Link

http://ashpublications.org/blood/article-pdf/91/1/368/1415538/368.pdf

Reference7 articles.

1. Hereditary spherocytosis and related disorders.;Becker;Clin Haematol,1985

2. β-spectrin Kissimmee: A spectrin variant associated with autossomal dominant hereditary spherocytosis and defective binding to protein 4.1.;Becker;J Clin Invest,1993

3. Molecular basis of spectrin deficiency in β spectrin Durham.;Hassoun;J Clin Invest,1995

4. Hereditary spherocytosis with spectrin deficiency due to an unstable truncated β spectrin.;Hassoun;Blood,1996

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