Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness-Reference-Cited by-同舟云学术

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

Published:2008-11-30 Issue:1 Volume:41 Page:106-111
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Lagresle-Peyrou Chantal,Six Emmanuelle M,Picard Capucine,Rieux-Laucat Frédéric,Michel Vincent,Ditadi Andrea,Chappedelaine Corinne Demerens-de,Morillon Estelle,Valensi Françoise,Simon-Stoos Karen L,Mullikin James C,Noroski Lenora M,Besse Céline,Wulffraat Nicolas M,Ferster Alina,Abecasis Manuel M,Calvo Fabien,Petit Christine,Candotti Fabio,Abel Laurent,Fischer Alain,Cavazzana-Calvo Marina

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.278.pdf

Reference26 articles.

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3. Reubsaet, L.L., Boelens, J.J., Rademaker, C., Smal, J. & Wulffraat, N.M. Successful cord blood transplantation in a premature and dysmature neonate of 1700 g with reticular dysgenesis. Bone Marrow Transplant. 39, 307–308 (2007).

4. Bujan, W., Ferster, A., Sariban, E. & Friedrich, W. Effect of recombinant human granulocyte colony-stimulating factor in reticular dysgenesis. Blood 82, 1684 (1993).

5. Antoine, C. et al. Long-term survival and transplantation of haemopoietic stem cells for immunodeficiencies: report of the European experience 1968–99. Lancet 361, 553–560 (2003).

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