Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness

Chantal Lagresle‐Peyrou(Inserm), Emmanuelle Six(Délégation Paris 5), Capucine Pïcard(Délégation Paris 5), Frédéric Rieux‐Laucat(Délégation Paris 5), Vincent Michel(Inserm), Andrea Ditadi(Délégation Paris 5), Corinne Demerens(Délégation Paris 5), Estelle Morillon(Délégation Paris 5), Françoise Valensi(Inserm), Karen L. Simon-Stoos(National Institutes of Health), James C. Mullikin(National Institutes of Health), Lenora M. Noroski(Baylor College of Medicine), Céline Besse(Commissariat à l'Énergie Atomique et aux Énergies Alternatives), N. M. Wulffraat(Wilhelmina Children's Hospital), Alina Ferster(Queen Fabiola Children's University Hospital), Manuel Abecasis(Instituto Português de Oncologia Francisco Gentil), Fabien Calvo(Inserm), Christine Petit(Inserm), Fabio Candotti(National Institutes of Health), Laurent Abel(Délégation Paris 5), Alain Fischer(Délégation Paris 5), Marina Cavazzana(Délégation Paris 5)
Nature Genetics
November 30, 2008
Cited by 238Open Access
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