Exome sequencing for diagnosis of congenital hemolytic anemia | Orphanet Journal of Rare Diseases | Full Text

Exome sequencing for diagnosis of congenital hemolytic anemia | Orphanet Journal of Rare Diseases | Full Text

Exome sequencing for diagnosis of congenital hemolytic anemia

Congenital hemolytic anemia constitutes a heterogeneous group of rare genetic disorders of red blood cells. Diagnosis is based on clinical data, family history and phenotypic testing, genetic analyses being us...

Authors:Lamisse Mansour-Hendili, Abdelrazak Aissat, Bouchra Badaoui, Mehdi Sakka, Christine Gameiro, Valérie Ortonne, Orianne Wagner-Ballon, Serge Pissard, Véronique Picard, Khaldoun Ghazal, Michel Bahuau, Corinne Guitton, Ziad Mansour, Mylène Duplan, Arnaud Petit, Nathalie Costedoat-Chalumeau…

Citation:Orphanet Journal of Rare Diseases 2020 15:180

Content type:Research

 

Published on: 8 July 2020

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