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Description and outcome of a cohort of 8 patients with WHIM syndrome from the French Severe Chronic Neutropenia Registry

<p>Abstract</p> <p>Background</p> <p>WHIM syndrome (WS), a rare congenital neutropenia due to mutations of the CXCR4 chemokine receptor, is associated with Human Papillomavirus (HPV)-induced Warts, Hypogammaglobulinemia, bacterial Infections and Myelokathexis. The long term follow up of eight patien...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Beaussant Cohen Sarah, Fenneteau Odile, Plouvier Emmanuel, Rohrlich Pierre-Simon, Daltroff Gerard, Plantier Isabelle, Dupuy Alain, Kerob Delphine, Beaupain Blandine, Bordigoni Pierre, Fouyssac Fanny, Delezoide Anne-Lise, Devouassoux Gilles, Nicolas Jean François, Bensaid Philippe, Bertrand Yves, Balabanian Karl, Chantelot Christine Bellanne, Bachelerie Françoise, Donadieu Jean
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BMC 2012-09-01
Sarja:Orphanet Journal of Rare Diseases
Aiheet:
Linkit:http://www.ojrd.com/content/7/1/71
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