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Hemoglobin
international journal for hemoglobin research
Volume 30, 2006 - Issue 1
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ORIGINAL ARTICLE

First Spanish Case Of Thalassemia Major Due to a Compound Heterozygosity for the IVS-II-848 (C→A) And Codon 39 (C→T) Mutations Of The β-Globin Gene

Paloma Ropero Servicio de Hematología y Hemoterapia, Hospital Clínico San Carlos de Madrid, Madrid, España
,
Ana Villegas Servicio de Hematología y Hemoterapia, Hospital Clínico San Carlos de Madrid, Madrid, EspañaCorrespondence[email protected]
,
Juan Muñoz Servicio de Hematología, Hospital Virgen del Mar de Cádiz, Cadiz, España
,
Olga Briceño Servicio de Hematología y Hemoterapia, Hospital Clínico San Carlos de Madrid, Madrid, España
,
Asunción Mora Servicio de Hematología y Hemoterapia, Hospital Clínico San Carlos de Madrid, Madrid, España
,
María Salvador Servicio de Hematología y Hemoterapia, Hospital Clínico San Carlos de Madrid, Madrid, España
,
Marta Polo Servicio de Hematología y Hemoterapia, Hospital Clínico San Carlos de Madrid, Madrid, España
&
Fernando A. González Servicio de Hematología y Hemoterapia, Hospital Clínico San Carlos de Madrid, Madrid, España
 show all
Pages 15-21 | Received 11 Jul 2005, Accepted 19 Sep 2005, Published online: 07 Jul 2009

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Read on this site (1)

Rakesh Kumar, Chandan Sagar, Dharmesh Sharma & Purnima Kishor. (2015) β-Globin Genes: Mutation Hot-Spots in the Global Thalassemia Belt. Hemoglobin 39:1, pages 1-8.
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Articles from other publishers (1)

F. Sinem Hocaoglu-Emre, Guven Yenmis, Devrim Saribal & Cengiz Yakicier. (2019) IVSII-74 T>G: As harmless as we thought?. Turkish Journal of Biochemistry 44:1, pages 41-46.
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