A novel <scp>α<sup>0</sup>‐thalassemia</scp> deletion in a Brazilian child with Hb H disease: −−<sup>Mococa</sup>-Reference-Cited by-同舟云学术

A novel α⁰‐thalassemia deletion in a Brazilian child with Hb H disease: −−^Mococa

Published:2024-04-03 Issue:4 Volume:46 Page:747-750
ISSN:1751-5521
Container-title:International Journal of Laboratory Hematology
language:en
Short-container-title:Int J Lab Hematology

Author:

Soler A. M.¹,Pedroso G. A.²,Geraldo A. P. M.³,Albuquerque D. M.⁴,Costa F. F.⁴,Santos M. N. N.²,Knijnenburg J.⁵,Harteveld C. L.⁵^ORCID,Sonati M. F.²,da Luz J. A.¹^ORCID

Affiliation:

1. Laboratorio de Genética Molecular Humana, Departamento de Ciencias Biológicas Centro Universitario Regional (CENUR) Litoral Norte. Universidad de la República (UdelaR) Salto Uruguay

2. Departamento de Patologia Clínica, Faculdade de Ciências Médicas Universidade Estadual de Campinas (UNICAMP) Campinas SP Brazil

3. Integrated Center for Oncohematological Research in Childhood (CIPOI) UNICAMP Campinas SP Brazil

4. Center for Hematology and Hemotherapy UNICAMP Campinas SP Brazil

5. Department of Human and Clinical Genetics, Hemoglobinopathy Expert Center Leiden University Medical Center‐LUMC Leiden The Netherlands

Funder

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Comisión Sectorial de Investigación Científica

Publisher

Wiley

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ijlh.14277

Reference12 articles.

1. Molecular basis of α-thalassemia

2. Inherited haemoglobin disorders: an increasing global health problem;Weatherall DJ;Bull World Health Organ,2001

3. Breakpoint characterization of a rare alpha 0 ‐thalassemia deletion using targeted locus amplification on genomic DNA

4. Simplified Multiplex-PCR Diagnosis of Common Southeast Asian Deletional Determinants of α-Thalassemia