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Nicolas Wulffraat
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Journal Articles

Human Adenylate Kinase 2 Deficiency Causes a Profound Haematopoietic Defect Associated with Sensorineural Deafness

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Marina Cavazzana-Calvo, MD, PhD, Chantal Lagresle-Peyrou, Emmanuelle M Six, Capucine Picard, MD, Frederic Rieux-Laucat, Vincent Michel, Andrea Ditadi, Corinne Demerens-de-Chappedelaine, Estelle Morillon, Françoise Valensi, Karen L Simon-Stoos, James C Mullikin, Lenora M Noroski, Céline Besse, Nicolas Wulffraat, Alina Ferster, MD, PhD, Manuel M Abecasis, MD, Fabien Calvo, MD, PhD, Christine Petit, PhD, Fabio Candotti, MD, Laurent Abel, PhD, Alain Fischer, MD, PhD
Journal: Blood
Blood (2008) 112 (11): lba-2.
https://doi.org/10.1182/blood.V112.11.lba-2.lba-2
Published: 2008
Journal Articles

Identical mutations in RAG1 or RAG2 genes leading to defective V(D)J recombinase activity can cause either T-B–severe combined immune deficiency or Omenn syndrome

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Clinical Trials & Observations
Barbara Corneo, Despina Moshous, Tayfun Güngör, Nicolas Wulffraat, Pierre Philippet, Françoise Le Deist, Alain Fischer, Jean-Pierre de Villartay
Journal: Blood
Blood (2001) 97 (9): 2772–2776.
https://doi.org/10.1182/blood.V97.9.2772
Published: 2001