Compound heterozygosity for the Cretan type of non-deletional hereditary persistence of fetal hemoglobin and β-thalassemia or Hb Sabine confirms the functional role of the Aγ −158 C>T mutation in γ-globin gene transcription-Reference-Cited by-同舟云学术

Compound heterozygosity for the Cretan type of non-deletional hereditary persistence of fetal hemoglobin and β-thalassemia or Hb Sabine confirms the functional role of the Aγ −158 C>T mutation in γ-globin gene transcription

Published:2008-11 Issue:3 Volume:41 Page:263-264
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Kollia Panagoula,Kalamaras Angelos,Chassanidis Christos,Samara Maria,Vamvakopoulos Nikolaos K.,Radmilovic Milena,Pavlovic Sonja,Papadakis Manoussos N.,Patrinos George P.

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference8 articles.

1. Hemoglobin switching;Stamatoyannopoulos,2001

2. The Cretan type of non-deletional hereditary persistence of fetal hemoglobin [Agamma −158 C>T] results from two independent gene conversion events;Patrinos;Hum. Genet.,1998

3. Contribution of gene conversion in the evolution of the human beta-like globin genes family;Papadakis;Hum. Genet.,1999

4. Genetic modifiers of beta-thalassemia;Thein;Haematologica,2005

5. Hemoglobin Sabine [beta91 (F7) Leu>Pro]: occurrence in a Sardinian individual with hemolytic anemia and inclusion bodies;Gasperini;Haematologica,1992

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