Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleClinical spectrum and long-term follow-up of 14 cases with G6PC3 mutations from the French severe congenital neutropenia registry.AuthorsDesplantes, Claire; Fremond, Marie Louise; Beaupain, Blandine; Harousseau, Jean Luc; Buzyn, Agnès; Pellier, Isabelle; Roques, Gaelle; Morville, Pierre; Paillard, Catherine; Bruneau, Julie; Pinson, Lucile; Jeziorski, Eric; Vannier, Jean Pierre; Picard, Capucine; Bellanger, Florence; Romero, Norma; de Pontual, Loïc; Lapillonne, Hélène; Lutz, Patrick; Chantelot, Christine BellannéPublicationOrphanet Journal of Rare Diseases, 2014, Vol 9, Issue 1, p183ISSN1750-1172Publication typeJournal ArticleDOI10.1186/s13023-014-0183-8