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Clinical spectrum and long-term follow-up of 14 cases with G6PC3 mutations from the French severe congenital neutropenia registry
Document Type
Article
Author
Desplantes, C.; Paillard, C.; Lutz, P.; Fremond, M.L.; De Pontual, L.; Beaupain, B.; Donadieu, J.; Harousseau, J.L.; Buzyn, A.; Pellier, I.; Roques, G.; Morville, P.; Bruneau, J.; Pinson, L.; Jeziorski, E.; Vannier, J.P.; Picard, C.; Bellanger, F.; Chantelot, C.B.; Romero, N.; Lapillonne, H.
Source
In: Orphanet Journal of Rare Diseases. (Orphanet Journal of Rare Diseases, 10 December 2014, 9(1))
Subject
Language
English
ISSN
17501172

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