Pyruvate kinase deficiency and severe congenital hemolytic anemia in a double heterozygous patient with paternal transmission of an early germ-linede novomutation-Reference-Cited by-同舟云学术

Pyruvate kinase deficiency and severe congenital hemolytic anemia in a double heterozygous patient with paternal transmission of an early germ-linede novomutation

Published:2015-11-17 Issue:12 Volume:90 Page:E217-E219
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am. J. Hematol.

Author:

Mañú-Pereira María Del Mar¹,Gonzalez-Roca Eva²,van Solinge Wouter W.³,Llaudet-Planas Esther¹,Sevilla Julián⁴,Montllor Laura¹,Mensa-Vilaro Anna²,Ploos van Amstel Hans Kristian⁵,van Wijk Richard³,Vives-Corrons JoanLluis¹

Affiliation:

1. Red Cell Pathology Unit; Hospital Clínic, IDIBAPS, University of Barcelona; Spain

2. Immunology Department; Hospital Clínic, IDIBAPS; Barcelona Spain

3. Department of Clinical Chemistry and Haematology; University Medical Center Utrecht; Utrecht the Netherlands

4. Department of Pediatrics; Hospital Niño Jesús; Madrid Spain

5. Department of Medical Genetics; University Medical Center Utrecht; Utrecht the Netherlands

Funder

Spanish Ministry of Economy and Competitiveness

Publisher

Wiley

Subject

Hematology