A new β0-thalassemia frameshift mutation [β 48 (-T)] in a Uruguayan family-Reference-Cited by-同舟云学术

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A new β0-thalassemia frameshift mutation [β 48 (-T)] in a Uruguayan family

Published:2012-08-17 Issue:1 Volume:35 Page:111-114
ISSN:1751-5521
Container-title:International Journal of Laboratory Hematology
language:en
Short-container-title:Int. Jnl. Lab. Hem.

Author:

Da Luz J.¹,López P.¹,Kimura E. M.²,Albuquerque D. M.³,Costa F. F.³,Sans M.⁴,Sonati M. F.²

Affiliation:

1. Departamento de Genética; Facultad de Medicina; Universidad de la República; Montevideo; Uruguay

2. Departamento de Patología Clinica; Faculdade de Ciências Médicas; Universidade Estadual de Campinas; Sao Paulo; Brazil

3. Hemocentro; Faculdade de Ciências Medicas; Universidade Estadual de Campinas; Sao Paulo; Brazil

4. Departmento de Antropología Biológica; Facultad de Humanidades y Ciencias de la Educación; Universidad de la República; Montevideo; Uruguay

Publisher

Wiley

Subject

Biochemistry, medical,Clinical Biochemistry,Hematology,General Medicine

Reference14 articles.

1. HbVar: a relational database of human hemoglobin variants and thalassemia mutations at the globin gene server;Hardison;Human Mutation,2002

2. Pi R Vidart D El legado de los inmigrantes 1969 1 60

3. Evaluating five dedicated automatic devices for haemoglobinopathy diagnostics in multi-ethnic populations;Van Delft;Int J Lab Hematol.,2009

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