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Exome sequencing for diagnosis of congenital hemolytic anemia
Document Type
Article
Author
Mansour-Hendili, L.; Aissat, A.; Sakka, M.; Gameiro, C.; Ortonne, V.; Pissard, S.; Bahuau, M.; Moutereau, S.; Funalot, B.; Wagner-Ballon, O.; Michel, M.; Bartolucci, P.; Galactéros, F.; Badaoui, B.; Picard, V.; Ghazal, K.; Guitton, C.; Mansour, Z.; Duplan, M.; Petit, A.; Costedoat-Chalumeau, N.
Source
In: Orphanet Journal of Rare Diseases. (Orphanet Journal of Rare Diseases, 8 July 2020, 15(1))
Subject
Language
English
ISSN
17501172

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