A Novel <i>PGM3</i> Mutation Is Associated With a Severe Phenotype of Bone Marrow Failure, Severe Combined Immunodeficiency, Skeletal Dysplasia, and Congenital Malformations
G. Pacheco-Cuellar(Centre Hospitalier Universitaire Sainte-Justine), Philippe M. Campeau(Centre Hospitalier Universitaire Sainte-Justine), Marlène Lemire-Girard(Centre Hospitalier Universitaire Sainte-Justine), Valérie Désilets(Centre Hospitalier Universitaire de Sherbrooke), Élie Haddad(Centre Hospitalier Universitaire Sainte-Justine), Michel Duval(Hôpital Robert-Debré), Christian Lachance(Centre Hospitalier Universitaire Sainte-Justine), Julie Gauthier(Centre Hospitalier Universitaire Sainte-Justine), Françoise Rypens(Centre Hospitalier Universitaire Sainte-Justine), Victor Kokta(Centre Hospitalier Universitaire Sainte-Justine), Hélène Decaluwe(Centre Hospitalier Universitaire Sainte-Justine), Françoise Le Deist(Centre National de la Recherche Scientifique), Dorothée Bouron‐Dal Soglio(Centre Hospitalier Universitaire Sainte-Justine)
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